Canonical Allele Identifier: CA430323861

Gene: COL5A2

Linked Data

• MyVariant Identifiers: chr2:g.189923577T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189058851T>G , CM000664.2:g.189058851T>G	GRCh38
NC_000002.11:g.189923577T>G , CM000664.1:g.189923577T>G	GRCh37
NC_000002.10:g.189631822T>G	NCBI36
NG_011799.1:g.126029A>C
NG_011799.2:g.126029A>C
NG_011799.3:g.171451A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374866.9:c.2128A>C MANE Select	ENSP00000364000.3:p.Arg710=
ENST00000374866.7:c.2128A>C	ENSP00000364000.3:p.Arg710=
ENST00000470524.2:n.234A>C
ENST00000618828.1:c.967A>C	ENSP00000482184.1:p.Arg323=
NM_000393.3:c.2128A>C	NP_000384.2:p.Arg710=
XM_011510573.1:c.1990A>C	XP_011508875.1:p.Arg664=
NM_000393.4:c.2128A>C	NP_000384.2:p.Arg710=
XM_011510573.3:c.1990A>C	XP_011508875.1:p.Arg664=
NM_000393.5:c.2128A>C MANE Select	NP_000384.2:p.Arg710=