Canonical Allele Identifier: CA518852609

Gene: GPC3

Linked Data

• gnomAD v4: X-133753836-A-G
• MyVariant Identifiers: chrX:g.132887863A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753836A>G , CM000685.2:g.133753836A>G	GRCh38
NC_000023.10:g.132887863A>G , CM000685.1:g.132887863A>G	GRCh37
NC_000023.9:g.132715529A>G	NCBI36
NG_009286.1:g.236804T>C , LRG_505:g.236804T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684880.1:c.*266T>C	ENSP00000510280.1:n.*266T>C
ENST00000689310.1:c.630T>C	ENSP00000510438.1:p.Thr210=
ENST00000370818.8:c.678T>C MANE Select	ENSP00000359854.3:p.Thr226=
ENST00000394299.7:c.678T>C	ENSP00000377836.2:p.Thr226=
ENST00000370818.7:c.678T>C	ENSP00000359854.3:p.Thr226=
ENST00000394299.6:c.678T>C	ENSP00000377836.2:p.Thr226=
ENST00000631057.2:c.516T>C	ENSP00000486325.1:p.Thr172=
NM_001164617.1:c.678T>C	NP_001158089.1:p.Thr226=
NM_001164618.1:c.630T>C	NP_001158090.1:p.Thr210=
NM_001164619.1:c.516T>C	NP_001158091.1:p.Thr172=
NM_004484.3:c.678T>C , LRG_505t1:c.678T>C	NP_004475.1:p.Thr226=
XM_017029413.2:c.678T>C	XP_016884902.1:p.Thr226=
NM_001164617.2:c.678T>C	NP_001158089.1:p.Thr226=
NM_001164618.2:c.630T>C	NP_001158090.1:p.Thr210=
NM_001164619.2:c.516T>C	NP_001158091.1:p.Thr172=
NM_004484.4:c.678T>C MANE Select	NP_004475.1:p.Thr226=