Canonical Allele Identifier: CA414706105

Gene: GPC3

Linked Data

• MyVariant Identifiers: chrX:g.132887865T>G (hg19) ; chrX:g.133753838T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753838T>G , CM000685.2:g.133753838T>G	GRCh38
NC_000023.10:g.132887865T>G , CM000685.1:g.132887865T>G	GRCh37
NC_000023.9:g.132715531T>G	NCBI36
NG_009286.1:g.236802A>C , LRG_505:g.236802A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684880.1:c.*264A>C	ENSP00000510280.1:n.*264A>C
ENST00000689310.1:c.628A>C	ENSP00000510438.1:p.Thr210Pro
ENST00000370818.8:c.676A>C MANE Select	ENSP00000359854.3:p.Thr226Pro
ENST00000394299.7:c.676A>C	ENSP00000377836.2:p.Thr226Pro
ENST00000370818.7:c.676A>C	ENSP00000359854.3:p.Thr226Pro
ENST00000394299.6:c.676A>C	ENSP00000377836.2:p.Thr226Pro
ENST00000631057.2:c.514A>C	ENSP00000486325.1:p.Thr172Pro
NM_001164617.1:c.676A>C	NP_001158089.1:p.Thr226Pro
NM_001164618.1:c.628A>C	NP_001158090.1:p.Thr210Pro
NM_001164619.1:c.514A>C	NP_001158091.1:p.Thr172Pro
NM_004484.3:c.676A>C , LRG_505t1:c.676A>C	NP_004475.1:p.Thr226Pro
XM_017029413.2:c.676A>C	XP_016884902.1:p.Thr226Pro
NM_001164617.2:c.676A>C	NP_001158089.1:p.Thr226Pro
NM_001164618.2:c.628A>C	NP_001158090.1:p.Thr210Pro
NM_001164619.2:c.514A>C	NP_001158091.1:p.Thr172Pro
NM_004484.4:c.676A>C MANE Select	NP_004475.1:p.Thr226Pro