Canonical Allele Identifier: CA430324398
Gene: COL5A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189927612A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189062886A>C , CM000664.2:g.189062886A>C GRCh38
NC_000002.11:g.189927612A>C , CM000664.1:g.189927612A>C GRCh37
NC_000002.10:g.189635857A>C NCBI36
NG_011799.1:g.121994T>G
NG_011799.2:g.121994T>G
NG_011799.3:g.167416T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.1956T>G MANE Select ENSP00000364000.3:p.Pro652=
ENST00000374866.7:c.1956T>G ENSP00000364000.3:p.Pro652=
ENST00000470524.2:n.62T>G
ENST00000618828.1:c.795T>G ENSP00000482184.1:p.Pro265=
NM_000393.3:c.1956T>G NP_000384.2:p.Pro652=
XM_011510573.1:c.1818T>G XP_011508875.1:p.Pro606=
NM_000393.4:c.1956T>G NP_000384.2:p.Pro652=
XM_011510573.3:c.1818T>G XP_011508875.1:p.Pro606=
NM_000393.5:c.1956T>G MANE Select NP_000384.2:p.Pro652=