Canonical Allele Identifier: CA13865220

Gene: GPC5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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