Canonical Allele Identifier: CA414705792
Gene: GPC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.133753716C>A , CM000685.2:g.133753716C>A GRCh38
NC_000023.10:g.132887743C>A , CM000685.1:g.132887743C>A GRCh37
NC_000023.9:g.132715409C>A NCBI36
NG_009286.1:g.236924G>T , LRG_505:g.236924G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684880.1:c.*386G>T ENSP00000510280.1:n.*386G>T
ENST00000689310.1:c.750G>T ENSP00000510438.1:p.Gln250His
ENST00000370818.8:c.798G>T MANE Select ENSP00000359854.3:p.Gln266His
ENST00000394299.7:c.798G>T ENSP00000377836.2:p.Gln266His
ENST00000370818.7:c.798G>T ENSP00000359854.3:p.Gln266His
ENST00000394299.6:c.798G>T ENSP00000377836.2:p.Gln266His
ENST00000631057.2:c.636G>T ENSP00000486325.1:p.Gln212His
NM_001164617.1:c.798G>T NP_001158089.1:p.Gln266His
NM_001164618.1:c.750G>T NP_001158090.1:p.Gln250His
NM_001164619.1:c.636G>T NP_001158091.1:p.Gln212His
NM_004484.3:c.798G>T , LRG_505t1:c.798G>T NP_004475.1:p.Gln266His
XM_017029413.2:c.798G>T XP_016884902.1:p.Gln266His
NM_001164617.2:c.798G>T NP_001158089.1:p.Gln266His
NM_001164618.2:c.750G>T NP_001158090.1:p.Gln250His
NM_001164619.2:c.636G>T NP_001158091.1:p.Gln212His
NM_004484.4:c.798G>T MANE Select NP_004475.1:p.Gln266His