Canonical Allele Identifier: CA414706083

Gene: GPC3

Linked Data

• MyVariant Identifiers: chrX:g.132887855A>G (hg19) ; chrX:g.133753828A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753828A>G , CM000685.2:g.133753828A>G	GRCh38
NC_000023.10:g.132887855A>G , CM000685.1:g.132887855A>G	GRCh37
NC_000023.9:g.132715521A>G	NCBI36
NG_009286.1:g.236812T>C , LRG_505:g.236812T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684880.1:c.*274T>C	ENSP00000510280.1:n.*274T>C
ENST00000689310.1:c.638T>C	ENSP00000510438.1:p.Phe213Ser
ENST00000370818.8:c.686T>C MANE Select	ENSP00000359854.3:p.Phe229Ser
ENST00000394299.7:c.686T>C	ENSP00000377836.2:p.Phe229Ser
ENST00000370818.7:c.686T>C	ENSP00000359854.3:p.Phe229Ser
ENST00000394299.6:c.686T>C	ENSP00000377836.2:p.Phe229Ser
ENST00000631057.2:c.524T>C	ENSP00000486325.1:p.Phe175Ser
NM_001164617.1:c.686T>C	NP_001158089.1:p.Phe229Ser
NM_001164618.1:c.638T>C	NP_001158090.1:p.Phe213Ser
NM_001164619.1:c.524T>C	NP_001158091.1:p.Phe175Ser
NM_004484.3:c.686T>C , LRG_505t1:c.686T>C	NP_004475.1:p.Phe229Ser
XM_017029413.2:c.686T>C	XP_016884902.1:p.Phe229Ser
NM_001164617.2:c.686T>C	NP_001158089.1:p.Phe229Ser
NM_001164618.2:c.638T>C	NP_001158090.1:p.Phe213Ser
NM_001164619.2:c.524T>C	NP_001158091.1:p.Phe175Ser
NM_004484.4:c.686T>C MANE Select	NP_004475.1:p.Phe229Ser