Canonical Allele Identifier: CA62600086
Gene: COL5A2 HGNC NCBI

Linked Data

dbSNP Id: rs35992256

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189058821dup , CM000664.2:g.189058821dup GRCh38
NC_000002.11:g.189923547dup , CM000664.1:g.189923547dup GRCh37
NC_000002.10:g.189631792dup NCBI36
NG_011799.1:g.126059dup
NG_011799.2:g.126059dup
NG_011799.3:g.171481dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.2130+28dup MANE Select ENSP00000364000.3:n.2130+28dup
ENST00000374866.7:c.2130+28dup ENSP00000364000.3:n.2130+28dup
ENST00000470524.2:n.236+28dup
ENST00000618828.1:c.969+28dup ENSP00000482184.1:n.969+28dup
NM_000393.3:c.2130+28dup NP_000384.2:n.2130+28dup
XM_011510573.1:c.1992+28dup XP_011508875.1:n.1992+28dup
NM_000393.4:c.2130+28dup NP_000384.2:n.2130+28dup
XM_011510573.3:c.1992+28dup XP_011508875.1:n.1992+28dup
NM_000393.5:c.2130+28dup MANE Select NP_000384.2:n.2130+28dup