Canonical Allele Identifier: CA2694733329

Gene: GPC3

Linked Data

• gnomAD v4: X-133952990-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133952990C>A , CM000685.2:g.133952990C>A	GRCh38
NC_000023.10:g.133087017C>A , CM000685.1:g.133087017C>A	GRCh37
NC_000023.9:g.132914683C>A	NCBI36
NG_009286.1:g.37650G>T , LRG_505:g.37650G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684880.1:c.337+60G>T	ENSP00000510280.1:n.337+60G>T
ENST00000689310.1:c.289+108G>T	ENSP00000510438.1:n.289+108G>T
ENST00000692630.1:n.467+60G>T
ENST00000370818.8:c.337+60G>T MANE Select	ENSP00000359854.3:n.337+60G>T
ENST00000394299.7:c.337+60G>T	ENSP00000377836.2:n.337+60G>T
ENST00000370818.7:c.337+60G>T	ENSP00000359854.3:n.337+60G>T
ENST00000394299.6:c.337+60G>T	ENSP00000377836.2:n.337+60G>T
ENST00000631057.2:c.175+32285G>T	ENSP00000486325.1:n.175+32285G>T
NM_001164617.1:c.337+60G>T	NP_001158089.1:n.337+60G>T
NM_001164618.1:c.289+108G>T	NP_001158090.1:n.289+108G>T
NM_001164619.1:c.175+32285G>T	NP_001158091.1:n.175+32285G>T
NM_004484.3:c.337+60G>T , LRG_505t1:c.337+60G>T	NP_004475.1:n.337+60G>T
XM_017029413.2:c.337+60G>T	XP_016884902.1:n.337+60G>T
NM_001164617.2:c.337+60G>T	NP_001158089.1:n.337+60G>T
NM_001164618.2:c.289+108G>T	NP_001158090.1:n.289+108G>T
NM_001164619.2:c.175+32285G>T	NP_001158091.1:n.175+32285G>T
NM_004484.4:c.337+60G>T MANE Select	NP_004475.1:n.337+60G>T