Canonical Allele Identifier: CA349876394
Gene: COL5A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189058886G>T , CM000664.2:g.189058886G>T GRCh38
NC_000002.11:g.189923612G>T , CM000664.1:g.189923612G>T GRCh37
NC_000002.10:g.189631857G>T NCBI36
NG_011799.1:g.125994C>A
NG_011799.2:g.125994C>A
NG_011799.3:g.171416C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000374866.9:c.2093C>A MANE Select ENSP00000364000.3:p.Pro698His
ENST00000374866.7:c.2093C>A ENSP00000364000.3:p.Pro698His
ENST00000470524.2:n.199C>A
ENST00000618828.1:c.932C>A ENSP00000482184.1:p.Pro311His
NM_000393.3:c.2093C>A NP_000384.2:p.Pro698His
XM_011510573.1:c.1955C>A XP_011508875.1:p.Pro652His
NM_000393.4:c.2093C>A NP_000384.2:p.Pro698His
XM_011510573.3:c.1955C>A XP_011508875.1:p.Pro652His
NM_000393.5:c.2093C>A MANE Select NP_000384.2:p.Pro698His