Canonical Allele Identifier: CA414706101

Gene: GPC3

Linked Data

• dbSNP Id: rs2124480324
• MyVariant Identifiers: chrX:g.132887864G>A (hg19) ; chrX:g.133753837G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753837G>A , CM000685.2:g.133753837G>A	GRCh38
NC_000023.10:g.132887864G>A , CM000685.1:g.132887864G>A	GRCh37
NC_000023.9:g.132715530G>A	NCBI36
NG_009286.1:g.236803C>T , LRG_505:g.236803C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000684880.1:c.*265C>T	ENSP00000510280.1:n.*265C>T
ENST00000689310.1:c.629C>T	ENSP00000510438.1:p.Thr210Ile
ENST00000370818.8:c.677C>T MANE Select	ENSP00000359854.3:p.Thr226Ile
ENST00000394299.7:c.677C>T	ENSP00000377836.2:p.Thr226Ile
ENST00000370818.7:c.677C>T	ENSP00000359854.3:p.Thr226Ile
ENST00000394299.6:c.677C>T	ENSP00000377836.2:p.Thr226Ile
ENST00000631057.2:c.515C>T	ENSP00000486325.1:p.Thr172Ile
NM_001164617.1:c.677C>T	NP_001158089.1:p.Thr226Ile
NM_001164618.1:c.629C>T	NP_001158090.1:p.Thr210Ile
NM_001164619.1:c.515C>T	NP_001158091.1:p.Thr172Ile
NM_004484.3:c.677C>T , LRG_505t1:c.677C>T	NP_004475.1:p.Thr226Ile
XM_017029413.2:c.677C>T	XP_016884902.1:p.Thr226Ile
NM_001164617.2:c.677C>T	NP_001158089.1:p.Thr226Ile
NM_001164618.2:c.629C>T	NP_001158090.1:p.Thr210Ile
NM_001164619.2:c.515C>T	NP_001158091.1:p.Thr172Ile
NM_004484.4:c.677C>T MANE Select	NP_004475.1:p.Thr226Ile