Canonical Allele Identifier: CA349866895

Gene: COL5A2

Linked Data

• gnomAD v4: 2-189050592-T-G
• MyVariant Identifiers: chr2:g.189915318T>G (hg19) ; chr2:g.189050592T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189050592T>G , CM000664.2:g.189050592T>G	GRCh38
NC_000002.11:g.189915318T>G , CM000664.1:g.189915318T>G	GRCh37
NC_000002.10:g.189623563T>G	NCBI36
NG_011799.1:g.134288A>C
NG_011799.2:g.134288A>C
NG_011799.3:g.179710A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374866.9:c.3016A>C MANE Select	ENSP00000364000.3:p.Met1006Leu
ENST00000374866.7:c.3016A>C	ENSP00000364000.3:p.Met1006Leu
ENST00000618828.1:c.1855A>C	ENSP00000482184.1:p.Met619Leu
NM_000393.3:c.3016A>C	NP_000384.2:p.Met1006Leu
XM_011510573.1:c.2878A>C	XP_011508875.1:p.Met960Leu
NM_000393.4:c.3016A>C	NP_000384.2:p.Met1006Leu
XM_011510573.3:c.2878A>C	XP_011508875.1:p.Met960Leu
NM_000393.5:c.3016A>C MANE Select	NP_000384.2:p.Met1006Leu