Canonical Allele Identifier: CA414705236

Gene: GPC3

Linked Data

• MyVariant Identifiers: chrX:g.132887613T>G (hg19) ; chrX:g.133753586T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753586T>G , CM000685.2:g.133753586T>G	GRCh38
NC_000023.10:g.132887613T>G , CM000685.1:g.132887613T>G	GRCh37
NC_000023.9:g.132715279T>G	NCBI36
NG_009286.1:g.237054A>C , LRG_505:g.237054A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406757.3:c.117A>C
ENST00000684880.1:c.*516A>C	ENSP00000510280.1:n.*516A>C
ENST00000689310.1:c.880A>C	ENSP00000510438.1:p.Met294Leu
ENST00000692084.1:c.122A>C
ENST00000370818.8:c.928A>C MANE Select	ENSP00000359854.3:p.Met310Leu
ENST00000394299.7:c.928A>C	ENSP00000377836.2:p.Met310Leu
ENST00000666673.1:n.122A>C
ENST00000370818.7:c.928A>C	ENSP00000359854.3:p.Met310Leu
ENST00000394299.6:c.928A>C	ENSP00000377836.2:p.Met310Leu
ENST00000406757.2:c.117A>C
ENST00000631057.2:c.766A>C	ENSP00000486325.1:p.Met256Leu
NM_001164617.1:c.928A>C	NP_001158089.1:p.Met310Leu
NM_001164618.1:c.880A>C	NP_001158090.1:p.Met294Leu
NM_001164619.1:c.766A>C	NP_001158091.1:p.Met256Leu
NM_004484.3:c.928A>C , LRG_505t1:c.928A>C	NP_004475.1:p.Met310Leu
XM_017029413.2:c.928A>C	XP_016884902.1:p.Met310Leu
NM_001164617.2:c.928A>C	NP_001158089.1:p.Met310Leu
NM_001164618.2:c.880A>C	NP_001158090.1:p.Met294Leu
NM_001164619.2:c.766A>C	NP_001158091.1:p.Met256Leu
NM_004484.4:c.928A>C MANE Select	NP_004475.1:p.Met310Leu