Canonical Allele Identifier: CA702334225

Gene: GPC5

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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