Canonical Allele Identifier: CA2110384814

Gene: GPC5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.91551559G= , CM000675.2:g.91551559G=	GRCh38
NC_000013.10:g.92203813G= , CM000675.1:g.92203813G=	GRCh37
NC_000013.9:g.91001814G=	NCBI36
NG_009370.1:g.157879G=
NG_009370.2:g.157879G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004466.6:c.325+102637G= MANE Select	NP_004457.1:n.325+102637G=
ENST00000377067.9:c.325+102637G= MANE Select	ENSP00000366267.3:n.325+102637G=
NM_004466.5:c.325+102637G=	NP_004457.1:n.325+102637G=
ENST00000377067.8:c.325+102637G=	ENSP00000366267.3:n.325+102637G=
XM_011521054.1:c.325+102637G=	XP_011519356.1:n.325+102637G=
XM_011521054.3:c.325+102637G=	XP_011519356.1:n.325+102637G=
XM_011521055.1:c.325+102637G=	XP_011519357.1:n.325+102637G=
XM_011521055.3:c.325+102637G=	XP_011519357.1:n.325+102637G=
XM_011521056.1:c.325+102637G=	XP_011519358.1:n.325+102637G=
XM_011521056.3:c.325+102637G=	XP_011519358.1:n.325+102637G=
XM_011521057.1:c.325+102637G=	XP_011519359.1:n.325+102637G=
XM_011521057.3:c.325+102637G=	XP_011519359.1:n.325+102637G=
XM_011521058.1:c.325+102637G=	XP_011519360.1:n.325+102637G=
XM_011521058.2:c.325+102637G=	XP_011519360.1:n.325+102637G=
XM_011521059.1:c.325+102637G=	XP_011519361.1:n.325+102637G=
XM_011521059.2:c.325+102637G=	XP_011519361.1:n.325+102637G=
XM_011521060.1:c.325+102637G=	XP_011519362.1:n.325+102637G=
XM_011521060.2:c.325+102637G=	XP_011519362.1:n.325+102637G=
XM_017020435.2:c.325+102637G=	XP_016875924.1:n.325+102637G=
XM_017020436.2:c.325+102637G=	XP_016875925.1:n.325+102637G=
XM_017020437.1:c.325+102637G=	XP_016875926.1:n.325+102637G=