Canonical Allele Identifier: CA2662314693

Gene: COL5A2

Linked Data

• gnomAD v4: 2-189062783-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189062783T>G , CM000664.2:g.189062783T>G	GRCh38
NC_000002.11:g.189927509T>G , CM000664.1:g.189927509T>G	GRCh37
NC_000002.10:g.189635754T>G	NCBI36
NG_011799.1:g.122097A>C
NG_011799.2:g.122097A>C
NG_011799.3:g.167519A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000374866.9:c.1977+82A>C MANE Select	ENSP00000364000.3:n.1977+82A>C
ENST00000374866.7:c.1977+82A>C	ENSP00000364000.3:n.1977+82A>C
ENST00000470524.2:n.83+82A>C
ENST00000618828.1:c.816+82A>C	ENSP00000482184.1:n.816+82A>C
NM_000393.3:c.1977+82A>C	NP_000384.2:n.1977+82A>C
XM_011510573.1:c.1839+82A>C	XP_011508875.1:n.1839+82A>C
NM_000393.4:c.1977+82A>C	NP_000384.2:n.1977+82A>C
XM_011510573.3:c.1839+82A>C	XP_011508875.1:n.1839+82A>C
NM_000393.5:c.1977+82A>C MANE Select	NP_000384.2:n.1977+82A>C