Canonical Allele Identifier: CA430324396
Gene: COL5A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189927609A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189062883A>T , CM000664.2:g.189062883A>T GRCh38
NC_000002.11:g.189927609A>T , CM000664.1:g.189927609A>T GRCh37
NC_000002.10:g.189635854A>T NCBI36
NG_011799.1:g.121997T>A
NG_011799.2:g.121997T>A
NG_011799.3:g.167419T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.1959T>A MANE Select ENSP00000364000.3:p.Ser653=
ENST00000374866.7:c.1959T>A ENSP00000364000.3:p.Ser653=
ENST00000470524.2:n.65T>A
ENST00000618828.1:c.798T>A ENSP00000482184.1:p.Ser266=
NM_000393.3:c.1959T>A NP_000384.2:p.Ser653=
XM_011510573.1:c.1821T>A XP_011508875.1:p.Ser607=
NM_000393.4:c.1959T>A NP_000384.2:p.Ser653=
XM_011510573.3:c.1821T>A XP_011508875.1:p.Ser607=
NM_000393.5:c.1959T>A MANE Select NP_000384.2:p.Ser653=