Canonical Allele Identifier: CA430322177

Gene: COL5A2

Linked Data

• MyVariant Identifiers: chr2:g.189915367G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189050641G>C , CM000664.2:g.189050641G>C	GRCh38
NC_000002.11:g.189915367G>C , CM000664.1:g.189915367G>C	GRCh37
NC_000002.10:g.189623612G>C	NCBI36
NG_011799.1:g.134239C>G
NG_011799.2:g.134239C>G
NG_011799.3:g.179661C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000374866.9:c.2967C>G MANE Select	ENSP00000364000.3:p.Thr989=
ENST00000374866.7:c.2967C>G	ENSP00000364000.3:p.Thr989=
ENST00000618828.1:c.1806C>G	ENSP00000482184.1:p.Thr602=
NM_000393.3:c.2967C>G	NP_000384.2:p.Thr989=
XM_011510573.1:c.2829C>G	XP_011508875.1:p.Thr943=
NM_000393.4:c.2967C>G	NP_000384.2:p.Thr989=
XM_011510573.3:c.2829C>G	XP_011508875.1:p.Thr943=
NM_000393.5:c.2967C>G MANE Select	NP_000384.2:p.Thr989=