Canonical Allele Identifier: CA518852546

Gene: GPC3

Linked Data

• MyVariant Identifiers: chrX:g.132888178A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133754151A>G , CM000685.2:g.133754151A>G	GRCh38
NC_000023.10:g.132888178A>G , CM000685.1:g.132888178A>G	GRCh37
NC_000023.9:g.132715844A>G	NCBI36
NG_009286.1:g.236489T>C , LRG_505:g.236489T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684880.1:c.434T>C	ENSP00000510280.1:p.Met145Thr
ENST00000689310.1:c.315T>C	ENSP00000510438.1:p.His105=
ENST00000692630.1:n.493T>C
ENST00000370818.8:c.363T>C MANE Select	ENSP00000359854.3:p.His121=
ENST00000394299.7:c.363T>C	ENSP00000377836.2:p.His121=
ENST00000370818.7:c.363T>C	ENSP00000359854.3:p.His121=
ENST00000394299.6:c.363T>C	ENSP00000377836.2:p.His121=
ENST00000631057.2:c.201T>C	ENSP00000486325.1:p.His67=
NM_001164617.1:c.363T>C	NP_001158089.1:p.His121=
NM_001164618.1:c.315T>C	NP_001158090.1:p.His105=
NM_001164619.1:c.201T>C	NP_001158091.1:p.His67=
NM_004484.3:c.363T>C , LRG_505t1:c.363T>C	NP_004475.1:p.His121=
XM_017029413.2:c.363T>C	XP_016884902.1:p.His121=
NM_001164617.2:c.363T>C	NP_001158089.1:p.His121=
NM_001164618.2:c.315T>C	NP_001158090.1:p.His105=
NM_001164619.2:c.201T>C	NP_001158091.1:p.His67=
NM_004484.4:c.363T>C MANE Select	NP_004475.1:p.His121=