Canonical Allele Identifier: CA414705885

Gene: GPC3

Linked Data

• MyVariant Identifiers: chrX:g.132887767T>A (hg19) ; chrX:g.133753740T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753740T>A , CM000685.2:g.133753740T>A	GRCh38
NC_000023.10:g.132887767T>A , CM000685.1:g.132887767T>A	GRCh37
NC_000023.9:g.132715433T>A	NCBI36
NG_009286.1:g.236900A>T , LRG_505:g.236900A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000684880.1:c.*362A>T	ENSP00000510280.1:n.*362A>T
ENST00000689310.1:c.726A>T	ENSP00000510438.1:p.Arg242Ser
ENST00000370818.8:c.774A>T MANE Select	ENSP00000359854.3:p.Arg258Ser
ENST00000394299.7:c.774A>T	ENSP00000377836.2:p.Arg258Ser
ENST00000370818.7:c.774A>T	ENSP00000359854.3:p.Arg258Ser
ENST00000394299.6:c.774A>T	ENSP00000377836.2:p.Arg258Ser
ENST00000631057.2:c.612A>T	ENSP00000486325.1:p.Arg204Ser
NM_001164617.1:c.774A>T	NP_001158089.1:p.Arg258Ser
NM_001164618.1:c.726A>T	NP_001158090.1:p.Arg242Ser
NM_001164619.1:c.612A>T	NP_001158091.1:p.Arg204Ser
NM_004484.3:c.774A>T , LRG_505t1:c.774A>T	NP_004475.1:p.Arg258Ser
XM_017029413.2:c.774A>T	XP_016884902.1:p.Arg258Ser
NM_001164617.2:c.774A>T	NP_001158089.1:p.Arg258Ser
NM_001164618.2:c.726A>T	NP_001158090.1:p.Arg242Ser
NM_001164619.2:c.612A>T	NP_001158091.1:p.Arg204Ser
NM_004484.4:c.774A>T MANE Select	NP_004475.1:p.Arg258Ser