Canonical Allele Identifier: CA414705119

Gene: GPC3

Linked Data

• MyVariant Identifiers: chrX:g.132887561A>G (hg19) ; chrX:g.133753534A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753534A>G , CM000685.2:g.133753534A>G	GRCh38
NC_000023.10:g.132887561A>G , CM000685.1:g.132887561A>G	GRCh37
NC_000023.9:g.132715227A>G	NCBI36
NG_009286.1:g.237106T>C , LRG_505:g.237106T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406757.3:c.169T>C
ENST00000684880.1:c.*568T>C	ENSP00000510280.1:n.*568T>C
ENST00000689310.1:c.932T>C	ENSP00000510438.1:p.Ile311Thr
ENST00000692084.1:c.174T>C
ENST00000370818.8:c.980T>C MANE Select	ENSP00000359854.3:p.Ile327Thr
ENST00000394299.7:c.980T>C	ENSP00000377836.2:p.Ile327Thr
ENST00000666673.1:n.174T>C
ENST00000370818.7:c.980T>C	ENSP00000359854.3:p.Ile327Thr
ENST00000394299.6:c.980T>C	ENSP00000377836.2:p.Ile327Thr
ENST00000406757.2:c.169T>C
ENST00000631057.2:c.818T>C	ENSP00000486325.1:p.Ile273Thr
NM_001164617.1:c.980T>C	NP_001158089.1:p.Ile327Thr
NM_001164618.1:c.932T>C	NP_001158090.1:p.Ile311Thr
NM_001164619.1:c.818T>C	NP_001158091.1:p.Ile273Thr
NM_004484.3:c.980T>C , LRG_505t1:c.980T>C	NP_004475.1:p.Ile327Thr
XM_017029413.2:c.980T>C	XP_016884902.1:p.Ile327Thr
NM_001164617.2:c.980T>C	NP_001158089.1:p.Ile327Thr
NM_001164618.2:c.932T>C	NP_001158090.1:p.Ile311Thr
NM_001164619.2:c.818T>C	NP_001158091.1:p.Ile273Thr
NM_004484.4:c.980T>C MANE Select	NP_004475.1:p.Ile327Thr