Canonical Allele Identifier: CA518852850

Gene: GPC3

Linked Data

• MyVariant Identifiers: chrX:g.132887770G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753743G>T , CM000685.2:g.133753743G>T	GRCh38
NC_000023.10:g.132887770G>T , CM000685.1:g.132887770G>T	GRCh37
NC_000023.9:g.132715436G>T	NCBI36
NG_009286.1:g.236897C>A , LRG_505:g.236897C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684880.1:c.*359C>A	ENSP00000510280.1:n.*359C>A
ENST00000689310.1:c.723C>A	ENSP00000510438.1:p.Thr241=
ENST00000370818.8:c.771C>A MANE Select	ENSP00000359854.3:p.Thr257=
ENST00000394299.7:c.771C>A	ENSP00000377836.2:p.Thr257=
ENST00000370818.7:c.771C>A	ENSP00000359854.3:p.Thr257=
ENST00000394299.6:c.771C>A	ENSP00000377836.2:p.Thr257=
ENST00000631057.2:c.609C>A	ENSP00000486325.1:p.Thr203=
NM_001164617.1:c.771C>A	NP_001158089.1:p.Thr257=
NM_001164618.1:c.723C>A	NP_001158090.1:p.Thr241=
NM_001164619.1:c.609C>A	NP_001158091.1:p.Thr203=
NM_004484.3:c.771C>A , LRG_505t1:c.771C>A	NP_004475.1:p.Thr257=
XM_017029413.2:c.771C>A	XP_016884902.1:p.Thr257=
NM_001164617.2:c.771C>A	NP_001158089.1:p.Thr257=
NM_001164618.2:c.723C>A	NP_001158090.1:p.Thr241=
NM_001164619.2:c.609C>A	NP_001158091.1:p.Thr203=
NM_004484.4:c.771C>A MANE Select	NP_004475.1:p.Thr257=