Canonical Allele Identifier: CA375173658

Gene: RALGPS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127174734C>T , CM000671.2:g.127174734C>T	GRCh38
NC_000009.11:g.129937013C>T , CM000671.1:g.129937013C>T	GRCh37
NC_000009.10:g.128976834C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259351.10:c.862C>T MANE Select	ENSP00000259351.5:p.Pro288Ser
ENST00000259351.9:c.862C>T	ENSP00000259351.5:p.Pro288Ser
ENST00000373434.5:c.862C>T	ENSP00000362533.1:p.Pro288Ser
ENST00000373436.5:c.862C>T	ENSP00000362535.1:p.Pro288Ser
ENST00000394022.7:c.862C>T	ENSP00000377590.3:p.Pro288Ser
ENST00000424082.6:c.862C>T	ENSP00000415630.2:p.Pro288Ser
NM_001190728.1:c.862C>T	NP_001177657.1:p.Pro288Ser
NM_001190729.1:c.862C>T	NP_001177658.1:p.Pro288Ser
NM_001190730.1:c.862C>T	NP_001177659.1:p.Pro288Ser
NM_014636.2:c.862C>T	NP_055451.1:p.Pro288Ser
XM_006717327.2:c.862C>T	XP_006717390.1:p.Pro288Ser
XM_006717328.2:c.1024C>T	XP_006717391.2:p.Pro342Ser
XM_011519225.1:c.1024C>T	XP_011517527.1:p.Pro342Ser
XM_011519226.1:c.1024C>T	XP_011517528.1:p.Pro342Ser
XM_011519227.1:c.973C>T	XP_011517529.1:p.Pro325Ser
XM_011519228.1:c.1024C>T	XP_011517530.1:p.Pro342Ser
XM_011519229.1:c.1024C>T	XP_011517531.1:p.Pro342Ser
XM_011519230.1:c.1024C>T	XP_011517532.1:p.Pro342Ser
XM_011519231.1:c.1024C>T	XP_011517533.1:p.Pro342Ser
XM_011519232.1:c.1024C>T	XP_011517534.1:p.Pro342Ser
XM_011519233.1:c.862C>T	XP_011517535.1:p.Pro288Ser
XM_011519234.1:c.934C>T	XP_011517536.1:p.Pro312Ser
XM_011519235.1:c.1024C>T	XP_011517537.1:p.Pro342Ser
XM_011519236.1:c.862C>T	XP_011517538.1:p.Pro288Ser
XM_011519237.1:c.1024C>T	XP_011517539.1:p.Pro342Ser
XM_011519238.1:c.1024C>T	XP_011517540.1:p.Pro342Ser
XM_011519239.1:c.601C>T	XP_011517541.1:p.Pro201Ser
XM_011519240.1:c.601C>T	XP_011517542.1:p.Pro201Ser
XR_929879.1:n.1089C>T
NM_001322320.1:c.862C>T	NP_001309249.1:p.Pro288Ser
NM_001322321.1:c.862C>T	NP_001309250.1:p.Pro288Ser
NM_001322322.1:c.862C>T	NP_001309251.1:p.Pro288Ser
NM_001322323.1:c.772C>T	NP_001309252.1:p.Pro258Ser
NM_001322324.1:c.862C>T	NP_001309253.1:p.Pro288Ser
NM_001322325.1:c.862C>T	NP_001309254.1:p.Pro288Ser
NM_001366400.1:c.862C>T	NP_001353329.1:p.Pro288Ser
NM_001366401.1:c.862C>T	NP_001353330.1:p.Pro288Ser
XM_006717328.3:c.1024C>T	XP_006717391.2:p.Pro342Ser
XM_011519230.2:c.1024C>T	XP_011517532.1:p.Pro342Ser
XM_011519234.2:c.934C>T	XP_011517536.1:p.Pro312Ser
XM_011519235.2:c.1024C>T	XP_011517537.1:p.Pro342Ser
XM_011519238.2:c.1024C>T	XP_011517540.1:p.Pro342Ser
XM_017015342.1:c.1024C>T	XP_016870831.1:p.Pro342Ser
XM_017015343.1:c.1024C>T	XP_016870832.1:p.Pro342Ser
XM_017015344.1:c.841C>T	XP_016870833.1:p.Pro281Ser
XM_017015345.1:c.1024C>T	XP_016870834.1:p.Pro342Ser
XM_017015346.1:c.862C>T	XP_016870835.1:p.Pro288Ser
XM_017015348.1:c.862C>T	XP_016870837.1:p.Pro288Ser
XM_017015349.1:c.601C>T	XP_016870838.1:p.Pro201Ser
XM_017015350.1:c.862C>T	XP_016870839.1:p.Pro288Ser
XR_001746426.1:n.1089C>T
NM_014636.3:c.862C>T MANE Select	NP_055451.1:p.Pro288Ser
NM_001190730.2:c.862C>T	NP_001177659.1:p.Pro288Ser
NM_001322320.2:c.862C>T	NP_001309249.1:p.Pro288Ser
NM_001322321.2:c.862C>T	NP_001309250.1:p.Pro288Ser
NM_001322322.2:c.862C>T	NP_001309251.1:p.Pro288Ser
NM_001322323.2:c.772C>T	NP_001309252.1:p.Pro258Ser
NM_001322324.2:c.862C>T	NP_001309253.1:p.Pro288Ser
NM_001322325.2:c.862C>T	NP_001309254.1:p.Pro288Ser
NM_001190729.2:c.862C>T	NP_001177658.1:p.Pro288Ser