Canonical Allele Identifier: CA349879022

Gene: COL5A2

Linked Data

• MyVariant Identifiers: chr2:g.189927616C>A (hg19) ; chr2:g.189062890C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189062890C>A , CM000664.2:g.189062890C>A	GRCh38
NC_000002.11:g.189927616C>A , CM000664.1:g.189927616C>A	GRCh37
NC_000002.10:g.189635861C>A	NCBI36
NG_011799.1:g.121990G>T
NG_011799.2:g.121990G>T
NG_011799.3:g.167412G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374866.9:c.1952G>T MANE Select	ENSP00000364000.3:p.Gly651Val
ENST00000374866.7:c.1952G>T	ENSP00000364000.3:p.Gly651Val
ENST00000470524.2:n.58G>T
ENST00000618828.1:c.791G>T	ENSP00000482184.1:p.Gly264Val
NM_000393.3:c.1952G>T	NP_000384.2:p.Gly651Val
XM_011510573.1:c.1814G>T	XP_011508875.1:p.Gly605Val
NM_000393.4:c.1952G>T	NP_000384.2:p.Gly651Val
XM_011510573.3:c.1814G>T	XP_011508875.1:p.Gly605Val
NM_000393.5:c.1952G>T MANE Select	NP_000384.2:p.Gly651Val