Canonical Allele Identifier: CA388460856

Gene: GPC5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.91399125G>A , CM000675.2:g.91399125G>A	GRCh38
NC_000013.10:g.92051379G>A , CM000675.1:g.92051379G>A	GRCh37
NC_000013.9:g.90849380G>A	NCBI36
NG_009370.1:g.5445G>A
NG_009370.2:g.5445G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004466.6:c.79G>A MANE Select	NP_004457.1:p.Val27Met
ENST00000377067.9:c.79G>A MANE Select	ENSP00000366267.3:p.Val27Met
NM_004466.5:c.79G>A	NP_004457.1:p.Val27Met
ENST00000377067.8:c.79G>A	ENSP00000366267.3:p.Val27Met
XM_011521054.1:c.79G>A	XP_011519356.1:p.Val27Met
XM_011521054.3:c.79G>A	XP_011519356.1:p.Val27Met
XM_011521055.1:c.79G>A	XP_011519357.1:p.Val27Met
XM_011521055.3:c.79G>A	XP_011519357.1:p.Val27Met
XM_011521056.1:c.79G>A	XP_011519358.1:p.Val27Met
XM_011521056.3:c.79G>A	XP_011519358.1:p.Val27Met
XM_011521057.1:c.79G>A	XP_011519359.1:p.Val27Met
XM_011521057.3:c.79G>A	XP_011519359.1:p.Val27Met
XM_011521058.1:c.79G>A	XP_011519360.1:p.Val27Met
XM_011521058.2:c.79G>A	XP_011519360.1:p.Val27Met
XM_011521059.1:c.79G>A	XP_011519361.1:p.Val27Met
XM_011521059.2:c.79G>A	XP_011519361.1:p.Val27Met
XM_011521060.1:c.79G>A	XP_011519362.1:p.Val27Met
XM_011521060.2:c.79G>A	XP_011519362.1:p.Val27Met
XM_017020435.2:c.79G>A	XP_016875924.1:p.Val27Met
XM_017020436.2:c.79G>A	XP_016875925.1:p.Val27Met
XM_017020437.1:c.79G>A	XP_016875926.1:p.Val27Met