Canonical Allele Identifier: CA2111694278

Gene: GPC6

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.94218552G= , CM000675.2:g.94218552G=	GRCh38
NC_000013.10:g.94870806G= , CM000675.1:g.94870806G=	GRCh37
NC_000013.9:g.93668807G=	NCBI36
NG_011880.1:g.996729G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377047.9:c.878-67797G= MANE Select	ENSP00000366246.3:n.878-67797G=
ENST00000377047.8:c.878-67797G=	ENSP00000366246.3:n.878-67797G=
NM_005708.3:c.878-67797G=	NP_005699.1:n.878-67797G=
XM_011521044.1:c.668-67797G=	XP_011519346.1:n.668-67797G=
NM_005708.4:c.878-67797G=	NP_005699.1:n.878-67797G=
XM_011521044.2:c.668-67797G=	XP_011519346.1:n.668-67797G=
XM_017020298.1:c.668-67797G=	XP_016875787.1:n.668-67797G=
XM_017020299.2:c.668-67797G=	XP_016875788.1:n.668-67797G=
XM_017020300.1:c.668-67797G=	XP_016875789.1:n.668-67797G=
XM_017020301.1:c.512-67797G=	XP_016875790.1:n.512-67797G=
XM_017020302.1:c.185-67797G=	XP_016875791.1:n.185-67797G=
NM_005708.5:c.878-67797G= MANE Select	NP_005699.1:n.878-67797G=