Canonical Allele Identifier: CA2532538233

Gene: GPC6

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.94218436T>A , CM000675.2:g.94218436T>A	GRCh38
NC_000013.10:g.94870690T>A , CM000675.1:g.94870690T>A	GRCh37
NC_000013.9:g.93668691T>A	NCBI36
NG_011880.1:g.996613T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000377047.9:c.878-67913T>A MANE Select	ENSP00000366246.3:n.878-67913T>A
ENST00000377047.8:c.878-67913T>A	ENSP00000366246.3:n.878-67913T>A
NM_005708.3:c.878-67913T>A	NP_005699.1:n.878-67913T>A
XM_011521044.1:c.668-67913T>A	XP_011519346.1:n.668-67913T>A
NM_005708.4:c.878-67913T>A	NP_005699.1:n.878-67913T>A
XM_011521044.2:c.668-67913T>A	XP_011519346.1:n.668-67913T>A
XM_017020298.1:c.668-67913T>A	XP_016875787.1:n.668-67913T>A
XM_017020299.2:c.668-67913T>A	XP_016875788.1:n.668-67913T>A
XM_017020300.1:c.668-67913T>A	XP_016875789.1:n.668-67913T>A
XM_017020301.1:c.512-67913T>A	XP_016875790.1:n.512-67913T>A
XM_017020302.1:c.185-67913T>A	XP_016875791.1:n.185-67913T>A
NM_005708.5:c.878-67913T>A MANE Select	NP_005699.1:n.878-67913T>A