Canonical Allele Identifier: CA414705897

Gene: GPC3

Linked Data

• ClinVar Variation Id: 2711914
• ClinVar RCV Id: RCV003501328
• MyVariant Identifiers: chrX:g.132887772T>A (hg19) ; chrX:g.133753745T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753745T>A , CM000685.2:g.133753745T>A	GRCh38
NC_000023.10:g.132887772T>A , CM000685.1:g.132887772T>A	GRCh37
NC_000023.9:g.132715438T>A	NCBI36
NG_009286.1:g.236895A>T , LRG_505:g.236895A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000684880.1:c.*357A>T	ENSP00000510280.1:n.*357A>T
ENST00000689310.1:c.721A>T	ENSP00000510438.1:p.Thr241Ser
ENST00000370818.8:c.769A>T MANE Select	ENSP00000359854.3:p.Thr257Ser
ENST00000394299.7:c.769A>T	ENSP00000377836.2:p.Thr257Ser
ENST00000370818.7:c.769A>T	ENSP00000359854.3:p.Thr257Ser
ENST00000394299.6:c.769A>T	ENSP00000377836.2:p.Thr257Ser
ENST00000631057.2:c.607A>T	ENSP00000486325.1:p.Thr203Ser
NM_001164617.1:c.769A>T	NP_001158089.1:p.Thr257Ser
NM_001164618.1:c.721A>T	NP_001158090.1:p.Thr241Ser
NM_001164619.1:c.607A>T	NP_001158091.1:p.Thr203Ser
NM_004484.3:c.769A>T , LRG_505t1:c.769A>T	NP_004475.1:p.Thr257Ser
XM_017029413.2:c.769A>T	XP_016884902.1:p.Thr257Ser
NM_001164617.2:c.769A>T	NP_001158089.1:p.Thr257Ser
NM_001164618.2:c.721A>T	NP_001158090.1:p.Thr241Ser
NM_001164619.2:c.607A>T	NP_001158091.1:p.Thr203Ser
NM_004484.4:c.769A>T MANE Select	NP_004475.1:p.Thr257Ser