Canonical Allele Identifier: CA5243545
Gene: RALGPS1 HGNC NCBI
ANGPTL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127108521C>T , CM000671.2:g.127108521C>T GRCh38
NC_000009.11:g.129870800C>T , CM000671.1:g.129870800C>T GRCh37
NC_000009.10:g.128910621C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000259351.10:c.610+39165C>T (RALGPS1) MANE Select ENSP00000259351.5:n.610+39165C>T
ENST00000373425.8:c.211G>A (ANGPTL2) MANE Select ENSP00000362524.3:p.Val71Ile
ENST00000259351.9:c.610+39165C>T (RALGPS1) ENSP00000259351.5:n.610+39165C>T
ENST00000373417.1:c.-90+13794G>A (ANGPTL2) ENSP00000362516.1:n.-90+13794G>A
ENST00000373425.7:c.211G>A (ANGPTL2) ENSP00000362524.3:p.Val71Ile
ENST00000373434.5:c.610+39165C>T (RALGPS1) ENSP00000362533.1:n.610+39165C>T
ENST00000373436.5:c.610+39165C>T (RALGPS1) ENSP00000362535.1:n.610+39165C>T
ENST00000394022.7:c.610+39165C>T (RALGPS1) ENSP00000377590.3:n.610+39165C>T
ENST00000424082.6:c.610+39165C>T (RALGPS1) ENSP00000415630.2:n.610+39165C>T
NM_001190728.1:c.610+39165C>T (RALGPS1) NP_001177657.1:n.610+39165C>T
NM_001190729.1:c.610+39165C>T (RALGPS1) NP_001177658.1:n.610+39165C>T
NM_001190730.1:c.610+39165C>T (RALGPS1) NP_001177659.1:n.610+39165C>T
NM_012098.2:c.211G>A (ANGPTL2) NP_036230.1:p.Val71Ile
NM_014636.2:c.610+39165C>T (RALGPS1) NP_055451.1:n.610+39165C>T
XM_006717030.2:c.211G>A (ANGPTL2) XP_006717093.1:p.Val71Ile
XM_006717327.2:c.610+39165C>T (RALGPS1) XP_006717390.1:n.610+39165C>T
XM_006717328.2:c.611-15093C>T (RALGPS1) XP_006717391.2:n.611-15093C>T
XM_011519225.1:c.611-15093C>T (RALGPS1) XP_011517527.1:n.611-15093C>T
XM_011519226.1:c.611-15093C>T (RALGPS1) XP_011517528.1:n.611-15093C>T
XM_011519227.1:c.560-15093C>T (RALGPS1) XP_011517529.1:n.560-15093C>T
XM_011519228.1:c.611-15093C>T (RALGPS1) XP_011517530.1:n.611-15093C>T
XM_011519229.1:c.611-15093C>T (RALGPS1) XP_011517531.1:n.611-15093C>T
XM_011519230.1:c.611-15093C>T (RALGPS1) XP_011517532.1:n.611-15093C>T
XM_011519231.1:c.611-15093C>T (RALGPS1) XP_011517533.1:n.611-15093C>T
XM_011519232.1:c.611-15093C>T (RALGPS1) XP_011517534.1:n.611-15093C>T
XM_011519233.1:c.610+39165C>T (RALGPS1) XP_011517535.1:n.610+39165C>T
XM_011519234.1:c.521-15093C>T (RALGPS1) XP_011517536.1:n.521-15093C>T
XM_011519235.1:c.611-15093C>T (RALGPS1) XP_011517537.1:n.611-15093C>T
XM_011519236.1:c.610+39165C>T (RALGPS1) XP_011517538.1:n.610+39165C>T
XM_011519237.1:c.611-15093C>T (RALGPS1) XP_011517539.1:n.611-15093C>T
XM_011519238.1:c.611-15093C>T (RALGPS1) XP_011517540.1:n.611-15093C>T
XM_011519239.1:c.188-15093C>T (RALGPS1) XP_011517541.1:n.188-15093C>T
XM_011519240.1:c.188-15093C>T (RALGPS1) XP_011517542.1:n.188-15093C>T
XR_929879.1:n.676-15093C>T (RALGPS1)
NM_001322320.1:c.610+39165C>T (RALGPS1) NP_001309249.1:n.610+39165C>T
NM_001322321.1:c.610+39165C>T (RALGPS1) NP_001309250.1:n.610+39165C>T
NM_001322322.1:c.610+39165C>T (RALGPS1) NP_001309251.1:n.610+39165C>T
NM_001322323.1:c.520+39165C>T (RALGPS1) NP_001309252.1:n.520+39165C>T
NM_001322324.1:c.610+39165C>T (RALGPS1) NP_001309253.1:n.610+39165C>T
NM_001322325.1:c.610+39165C>T (RALGPS1) NP_001309254.1:n.610+39165C>T
NM_001366400.1:c.610+39165C>T (RALGPS1) NP_001353329.1:n.610+39165C>T
NM_001366401.1:c.610+39165C>T (RALGPS1) NP_001353330.1:n.610+39165C>T
XM_006717030.4:c.211G>A (ANGPTL2) XP_006717093.1:p.Val71Ile
XM_006717328.3:c.611-15093C>T (RALGPS1) XP_006717391.2:n.611-15093C>T
XM_011519230.2:c.611-15093C>T (RALGPS1) XP_011517532.1:n.611-15093C>T
XM_011519234.2:c.521-15093C>T (RALGPS1) XP_011517536.1:n.521-15093C>T
XM_011519235.2:c.611-15093C>T (RALGPS1) XP_011517537.1:n.611-15093C>T
XM_011519238.2:c.611-15093C>T (RALGPS1) XP_011517540.1:n.611-15093C>T
XM_017015342.1:c.611-15093C>T (RALGPS1) XP_016870831.1:n.611-15093C>T
XM_017015343.1:c.611-15093C>T (RALGPS1) XP_016870832.1:n.611-15093C>T
XM_017015344.1:c.428-15093C>T (RALGPS1) XP_016870833.1:n.428-15093C>T
XM_017015345.1:c.611-15093C>T (RALGPS1) XP_016870834.1:n.611-15093C>T
XM_017015346.1:c.610+39165C>T (RALGPS1) XP_016870835.1:n.610+39165C>T
XM_017015348.1:c.610+39165C>T (RALGPS1) XP_016870837.1:n.610+39165C>T
XM_017015349.1:c.188-15093C>T (RALGPS1) XP_016870838.1:n.188-15093C>T
XM_017015350.1:c.610+39165C>T (RALGPS1) XP_016870839.1:n.610+39165C>T
XR_001746426.1:n.676-15093C>T (RALGPS1)
NM_012098.3:c.211G>A (ANGPTL2) MANE Select NP_036230.1:p.Val71Ile
NM_014636.3:c.610+39165C>T (RALGPS1) MANE Select NP_055451.1:n.610+39165C>T
NM_001190730.2:c.610+39165C>T (RALGPS1) NP_001177659.1:n.610+39165C>T
NM_001322320.2:c.610+39165C>T (RALGPS1) NP_001309249.1:n.610+39165C>T
NM_001322321.2:c.610+39165C>T (RALGPS1) NP_001309250.1:n.610+39165C>T
NM_001322322.2:c.610+39165C>T (RALGPS1) NP_001309251.1:n.610+39165C>T
NM_001322323.2:c.520+39165C>T (RALGPS1) NP_001309252.1:n.520+39165C>T
NM_001322324.2:c.610+39165C>T (RALGPS1) NP_001309253.1:n.610+39165C>T
NM_001322325.2:c.610+39165C>T (RALGPS1) NP_001309254.1:n.610+39165C>T
NM_001190729.2:c.610+39165C>T (RALGPS1) NP_001177658.1:n.610+39165C>T