Canonical Allele Identifier: CA3238984
Community Standard Title: NM_001384732.1(CPLANE1):c.3234A>G (p.Gln1078=)
Gene: CPLANE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37205370T>C , CM000667.2:g.37205370T>C GRCh38
NC_000005.9:g.37205472T>C , CM000667.1:g.37205472T>C GRCh37
NC_000005.8:g.37241229T>C NCBI36
NG_032772.1:g.49059A>G
NG_032772.2:g.49059A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001384732.1:c.3234A>G MANE Select NP_001371661.1:p.Gln1078=
ENST00000651892.2:c.3234A>G MANE Select ENSP00000498265.2:p.Gln1078=
NM_023073.3:c.3234A>G NP_075561.3:p.Gln1078=
NM_023073.4:c.3234A>G NP_075561.3:p.Gln1078=
ENST00000425232.6:c.3234A>G ENSP00000389014.2:p.Gln1078=
ENST00000425232.7:c.2738A>G
ENST00000505431.1:n.271A>G
ENST00000508244.5:c.3234A>G ENSP00000421690.1:p.Gln1078=
ENST00000509849.5:c.249A>G ENSP00000426337.1:p.Gln83=
ENST00000514429.5:c.378A>G ENSP00000424223.1:p.Gln126=
ENST00000675547.1:n.3304A>G
ENST00000676290.1:n.3309A>G
XM_005248345.2:c.3234A>G XP_005248402.1:p.Gln1078=
XM_005248345.4:c.3234A>G XP_005248402.1:p.Gln1078=
XM_005248346.2:c.3234A>G XP_005248403.1:p.Gln1078=
XM_005248346.4:c.3234A>G XP_005248403.1:p.Gln1078=
XM_005248347.2:c.3234A>G XP_005248404.1:p.Gln1078=
XM_005248347.4:c.3234A>G XP_005248404.1:p.Gln1078=
XM_005248349.2:c.3234A>G XP_005248406.1:p.Gln1078=
XM_005248349.4:c.3234A>G XP_005248406.1:p.Gln1078=
XM_005248350.2:c.3105A>G XP_005248407.1:p.Gln1035=
XM_005248350.4:c.3105A>G XP_005248407.1:p.Gln1035=
XM_006714489.2:c.3234A>G XP_006714552.1:p.Gln1078=
XM_011514085.1:c.3234A>G XP_011512387.1:p.Gln1078=
XM_011514085.3:c.3234A>G XP_011512387.1:p.Gln1078=
XM_011514086.1:c.3234A>G XP_011512388.1:p.Gln1078=
XM_011514086.3:c.3234A>G XP_011512388.1:p.Gln1078=
XM_011514087.1:c.3234A>G XP_011512389.1:p.Gln1078=
XM_011514087.2:c.3234A>G XP_011512389.1:p.Gln1078=
XM_011514088.1:c.3234A>G XP_011512390.1:p.Gln1078=
XM_011514088.2:c.3234A>G XP_011512390.1:p.Gln1078=
XM_011514089.1:c.3234A>G XP_011512391.1:p.Gln1078=
XM_011514089.2:c.3234A>G XP_011512391.1:p.Gln1078=
XM_011514090.1:c.2916A>G XP_011512392.1:p.Gln972=
XM_011514090.3:c.2916A>G XP_011512392.1:p.Gln972=
XM_011514091.1:c.2562A>G XP_011512393.1:p.Gln854=
XM_011514092.1:c.3234A>G XP_011512394.1:p.Gln1078=
XM_011514092.2:c.3234A>G XP_011512394.1:p.Gln1078=
XM_011514093.1:c.3234A>G XP_011512395.1:p.Gln1078=
XM_011514094.1:c.459A>G XP_011512396.1:p.Gln153=
XM_011514094.2:c.459A>G XP_011512396.1:p.Gln153=
XM_017009760.1:c.3045A>G XP_016865249.1:p.Gln1015=
XM_017009761.2:c.3045A>G XP_016865250.1:p.Gln1015=
XM_017009763.1:c.2241A>G XP_016865252.1:p.Gln747=
XM_017009765.1:c.2046A>G XP_016865254.1:p.Gln682=
XM_017009766.1:c.-271A>G XP_016865255.1:n.-271A>G
XM_024446183.1:c.3045A>G XP_024301951.1:p.Gln1015=
XM_024446184.1:c.2916A>G XP_024301952.1:p.Gln972=
XM_024446185.1:c.2562A>G XP_024301953.1:p.Gln854=
XM_024446186.1:c.2241A>G XP_024301954.1:p.Gln747=
XR_001742208.1:n.3458A>G
XR_002956171.1:n.3458A>G
XR_427661.2:n.3409A>G
XR_925644.1:n.3409A>G
XR_925644.2:n.3458A>G