Canonical Allele Identifier: CA430323862

Gene: COL5A2

Linked Data

• MyVariant Identifiers: chr2:g.189923578A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189058852A>C , CM000664.2:g.189058852A>C	GRCh38
NC_000002.11:g.189923578A>C , CM000664.1:g.189923578A>C	GRCh37
NC_000002.10:g.189631823A>C	NCBI36
NG_011799.1:g.126028T>G
NG_011799.2:g.126028T>G
NG_011799.3:g.171450T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374866.9:c.2127T>G MANE Select	ENSP00000364000.3:p.Pro709=
ENST00000374866.7:c.2127T>G	ENSP00000364000.3:p.Pro709=
ENST00000470524.2:n.233T>G
ENST00000618828.1:c.966T>G	ENSP00000482184.1:p.Pro322=
NM_000393.3:c.2127T>G	NP_000384.2:p.Pro709=
XM_011510573.1:c.1989T>G	XP_011508875.1:p.Pro663=
NM_000393.4:c.2127T>G	NP_000384.2:p.Pro709=
XM_011510573.3:c.1989T>G	XP_011508875.1:p.Pro663=
NM_000393.5:c.2127T>G MANE Select	NP_000384.2:p.Pro709=