Canonical Allele Identifier: CA414706090

Gene: GPC3

Linked Data

• MyVariant Identifiers: chrX:g.132887858A>G (hg19) ; chrX:g.133753831A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753831A>G , CM000685.2:g.133753831A>G	GRCh38
NC_000023.10:g.132887858A>G , CM000685.1:g.132887858A>G	GRCh37
NC_000023.9:g.132715524A>G	NCBI36
NG_009286.1:g.236809T>C , LRG_505:g.236809T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684880.1:c.*271T>C	ENSP00000510280.1:n.*271T>C
ENST00000689310.1:c.635T>C	ENSP00000510438.1:p.Ile212Thr
ENST00000370818.8:c.683T>C MANE Select	ENSP00000359854.3:p.Ile228Thr
ENST00000394299.7:c.683T>C	ENSP00000377836.2:p.Ile228Thr
ENST00000370818.7:c.683T>C	ENSP00000359854.3:p.Ile228Thr
ENST00000394299.6:c.683T>C	ENSP00000377836.2:p.Ile228Thr
ENST00000631057.2:c.521T>C	ENSP00000486325.1:p.Ile174Thr
NM_001164617.1:c.683T>C	NP_001158089.1:p.Ile228Thr
NM_001164618.1:c.635T>C	NP_001158090.1:p.Ile212Thr
NM_001164619.1:c.521T>C	NP_001158091.1:p.Ile174Thr
NM_004484.3:c.683T>C , LRG_505t1:c.683T>C	NP_004475.1:p.Ile228Thr
XM_017029413.2:c.683T>C	XP_016884902.1:p.Ile228Thr
NM_001164617.2:c.683T>C	NP_001158089.1:p.Ile228Thr
NM_001164618.2:c.635T>C	NP_001158090.1:p.Ile212Thr
NM_001164619.2:c.521T>C	NP_001158091.1:p.Ile174Thr
NM_004484.4:c.683T>C MANE Select	NP_004475.1:p.Ile228Thr