Canonical Allele Identifier: CA414699461

Gene: GPC3

Linked Data

• MyVariant Identifiers: chrX:g.132833941G>T (hg19) ; chrX:g.133699913G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133699913G>T , CM000685.2:g.133699913G>T	GRCh38
NC_000023.10:g.132833941G>T , CM000685.1:g.132833941G>T	GRCh37
NC_000023.9:g.132661607G>T	NCBI36
NG_009286.1:g.290726C>A , LRG_505:g.290726C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406757.3:c.337C>A
ENST00000666673.2:n.179C>A
ENST00000684880.1:c.*736C>A	ENSP00000510280.1:n.*736C>A
ENST00000689310.1:c.1100C>A	ENSP00000510438.1:p.Thr367Asn
ENST00000692084.1:c.435C>A
ENST00000370818.8:c.1148C>A MANE Select	ENSP00000359854.3:p.Thr383Asn
ENST00000394299.7:c.1217C>A	ENSP00000377836.2:p.Thr406Asn
ENST00000666673.1:n.435C>A
ENST00000667662.1:n.215C>A
ENST00000669691.1:n.194C>A
ENST00000370818.7:c.1148C>A	ENSP00000359854.3:p.Thr383Asn
ENST00000394299.6:c.1217C>A	ENSP00000377836.2:p.Thr406Asn
ENST00000406757.2:c.337C>A
ENST00000631057.2:c.986C>A	ENSP00000486325.1:p.Thr329Asn
NM_001164617.1:c.1217C>A	NP_001158089.1:p.Thr406Asn
NM_001164618.1:c.1100C>A	NP_001158090.1:p.Thr367Asn
NM_001164619.1:c.986C>A	NP_001158091.1:p.Thr329Asn
NM_004484.3:c.1148C>A , LRG_505t1:c.1148C>A	NP_004475.1:p.Thr383Asn
XM_017029413.2:c.1148C>A	XP_016884902.1:p.Thr383Asn
NM_001164617.2:c.1217C>A	NP_001158089.1:p.Thr406Asn
NM_001164618.2:c.1100C>A	NP_001158090.1:p.Thr367Asn
NM_001164619.2:c.986C>A	NP_001158091.1:p.Thr329Asn
NM_004484.4:c.1148C>A MANE Select	NP_004475.1:p.Thr383Asn