Canonical Allele Identifier: CA349866779

Gene: COL5A2

Linked Data

• MyVariant Identifiers: chr2:g.189915297C>G (hg19) ; chr2:g.189050571C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189050571C>G , CM000664.2:g.189050571C>G	GRCh38
NC_000002.11:g.189915297C>G , CM000664.1:g.189915297C>G	GRCh37
NC_000002.10:g.189623542C>G	NCBI36
NG_011799.1:g.134309G>C
NG_011799.2:g.134309G>C
NG_011799.3:g.179731G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374866.9:c.3037G>C MANE Select	ENSP00000364000.3:p.Ala1013Pro
ENST00000374866.7:c.3037G>C	ENSP00000364000.3:p.Ala1013Pro
ENST00000618828.1:c.1876G>C	ENSP00000482184.1:p.Ala626Pro
NM_000393.3:c.3037G>C	NP_000384.2:p.Ala1013Pro
XM_011510573.1:c.2899G>C	XP_011508875.1:p.Ala967Pro
NM_000393.4:c.3037G>C	NP_000384.2:p.Ala1013Pro
XM_011510573.3:c.2899G>C	XP_011508875.1:p.Ala967Pro
NM_000393.5:c.3037G>C MANE Select	NP_000384.2:p.Ala1013Pro