Canonical Allele Identifier: CA2018061163

Gene: GPC5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.91792975C= , CM000675.2:g.91792975C=	GRCh38
NC_000013.10:g.92445229C= , CM000675.1:g.92445229C=	GRCh37
NC_000013.9:g.91243230C=	NCBI36
NG_009370.1:g.399295C=
NG_009370.2:g.399295C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004466.6:c.1280+36555C= MANE Select	NP_004457.1:n.1280+36555C=
ENST00000377067.9:c.1280+36555C= MANE Select	ENSP00000366267.3:n.1280+36555C=
NM_004466.5:c.1280+36555C=	NP_004457.1:n.1280+36555C=
ENST00000377067.8:c.1280+36555C=	ENSP00000366267.3:n.1280+36555C=
XM_011521054.1:c.1280+36555C=	XP_011519356.1:n.1280+36555C=
XM_011521054.3:c.1280+36555C=	XP_011519356.1:n.1280+36555C=
XM_011521058.1:c.*25+28119C=	XP_011519360.1:n.*25+28119C=
XM_011521058.2:c.*25+28119C=	XP_011519360.1:n.*25+28119C=
XM_011521059.1:c.*25+28119C=	XP_011519361.1:n.*25+28119C=
XM_011521059.2:c.*25+28119C=	XP_011519361.1:n.*25+28119C=
XM_011521060.1:c.1281-30422C=	XP_011519362.1:n.1281-30422C=
XM_011521060.2:c.1281-30422C=	XP_011519362.1:n.1281-30422C=
XM_017020435.2:c.1280+36555C=	XP_016875924.1:n.1280+36555C=
XM_017020437.1:c.*25+28119C=	XP_016875926.1:n.*25+28119C=