Canonical Allele Identifier: CA414706071

Gene: GPC3

Linked Data

• MyVariant Identifiers: chrX:g.132887850G>A (hg19) ; chrX:g.133753823G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753823G>A , CM000685.2:g.133753823G>A	GRCh38
NC_000023.10:g.132887850G>A , CM000685.1:g.132887850G>A	GRCh37
NC_000023.9:g.132715516G>A	NCBI36
NG_009286.1:g.236817C>T , LRG_505:g.236817C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000684880.1:c.*279C>T	ENSP00000510280.1:n.*279C>T
ENST00000689310.1:c.643C>T	ENSP00000510438.1:p.Gln215Ter
ENST00000370818.8:c.691C>T MANE Select	ENSP00000359854.3:p.Gln231Ter
ENST00000394299.7:c.691C>T	ENSP00000377836.2:p.Gln231Ter
ENST00000370818.7:c.691C>T	ENSP00000359854.3:p.Gln231Ter
ENST00000394299.6:c.691C>T	ENSP00000377836.2:p.Gln231Ter
ENST00000631057.2:c.529C>T	ENSP00000486325.1:p.Gln177Ter
NM_001164617.1:c.691C>T	NP_001158089.1:p.Gln231Ter
NM_001164618.1:c.643C>T	NP_001158090.1:p.Gln215Ter
NM_001164619.1:c.529C>T	NP_001158091.1:p.Gln177Ter
NM_004484.3:c.691C>T , LRG_505t1:c.691C>T	NP_004475.1:p.Gln231Ter
XM_017029413.2:c.691C>T	XP_016884902.1:p.Gln231Ter
NM_001164617.2:c.691C>T	NP_001158089.1:p.Gln231Ter
NM_001164618.2:c.643C>T	NP_001158090.1:p.Gln215Ter
NM_001164619.2:c.529C>T	NP_001158091.1:p.Gln177Ter
NM_004484.4:c.691C>T MANE Select	NP_004475.1:p.Gln231Ter