Canonical Allele Identifier: CA349876353
Gene: COL5A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189058880T>C , CM000664.2:g.189058880T>C GRCh38
NC_000002.11:g.189923606T>C , CM000664.1:g.189923606T>C GRCh37
NC_000002.10:g.189631851T>C NCBI36
NG_011799.1:g.126000A>G
NG_011799.2:g.126000A>G
NG_011799.3:g.171422A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000374866.9:c.2099A>G MANE Select ENSP00000364000.3:p.Asp700Gly
ENST00000374866.7:c.2099A>G ENSP00000364000.3:p.Asp700Gly
ENST00000470524.2:n.205A>G
ENST00000618828.1:c.938A>G ENSP00000482184.1:p.Asp313Gly
NM_000393.3:c.2099A>G NP_000384.2:p.Asp700Gly
XM_011510573.1:c.1961A>G XP_011508875.1:p.Asp654Gly
NM_000393.4:c.2099A>G NP_000384.2:p.Asp700Gly
XM_011510573.3:c.1961A>G XP_011508875.1:p.Asp654Gly
NM_000393.5:c.2099A>G MANE Select NP_000384.2:p.Asp700Gly