Canonical Allele Identifier: CA430442483

Gene: COL5A2

Linked Data

• MyVariant Identifiers: chr2:g.189899843A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189035117A>T , CM000664.2:g.189035117A>T	GRCh38
NC_000002.11:g.189899843A>T , CM000664.1:g.189899843A>T	GRCh37
NC_000002.10:g.189608088A>T	NCBI36
NG_011799.1:g.149763T>A
NG_011799.2:g.149763T>A
NG_011799.3:g.195185T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374866.9:c.4152T>A MANE Select	ENSP00000364000.3:p.Ile1384=
ENST00000374866.7:c.4152T>A	ENSP00000364000.3:p.Ile1384=
ENST00000618828.1:c.2991T>A	ENSP00000482184.1:p.Ile997=
NM_000393.3:c.4152T>A	NP_000384.2:p.Ile1384=
XM_011510573.1:c.4014T>A	XP_011508875.1:p.Ile1338=
NM_000393.4:c.4152T>A	NP_000384.2:p.Ile1384=
XM_011510573.3:c.4014T>A	XP_011508875.1:p.Ile1338=
NM_000393.5:c.4152T>A MANE Select	NP_000384.2:p.Ile1384=