Canonical Allele Identifier: CA349879080

Gene: COL5A2

Linked Data

• MyVariant Identifiers: chr2:g.189927625C>T (hg19) ; chr2:g.189062899C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189062899C>T , CM000664.2:g.189062899C>T	GRCh38
NC_000002.11:g.189927625C>T , CM000664.1:g.189927625C>T	GRCh37
NC_000002.10:g.189635870C>T	NCBI36
NG_011799.1:g.121981G>A
NG_011799.2:g.121981G>A
NG_011799.3:g.167403G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374866.9:c.1943G>A MANE Select	ENSP00000364000.3:p.Gly648Asp
ENST00000374866.7:c.1943G>A	ENSP00000364000.3:p.Gly648Asp
ENST00000470524.2:n.49G>A
ENST00000618828.1:c.782G>A	ENSP00000482184.1:p.Gly261Asp
NM_000393.3:c.1943G>A	NP_000384.2:p.Gly648Asp
XM_011510573.1:c.1805G>A	XP_011508875.1:p.Gly602Asp
NM_000393.4:c.1943G>A	NP_000384.2:p.Gly648Asp
XM_011510573.3:c.1805G>A	XP_011508875.1:p.Gly602Asp
NM_000393.5:c.1943G>A MANE Select	NP_000384.2:p.Gly648Asp