Canonical Allele Identifier: CA2662314123
Gene: COL5A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189058782dup , CM000664.2:g.189058782dup GRCh38
NC_000002.11:g.189923508dup , CM000664.1:g.189923508dup GRCh37
NC_000002.10:g.189631753dup NCBI36
NG_011799.1:g.126101dup
NG_011799.2:g.126101dup
NG_011799.3:g.171523dup

Transcript Alleles

HGVS Amino-acid change
ENST00000374866.9:c.2130+70dup MANE Select ENSP00000364000.3:n.2130+70dup
ENST00000374866.7:c.2130+70dup ENSP00000364000.3:n.2130+70dup
ENST00000470524.2:n.236+70dup
ENST00000618828.1:c.969+70dup ENSP00000482184.1:n.969+70dup
NM_000393.3:c.2130+70dup NP_000384.2:n.2130+70dup
XM_011510573.1:c.1992+70dup XP_011508875.1:n.1992+70dup
NM_000393.4:c.2130+70dup NP_000384.2:n.2130+70dup
XM_011510573.3:c.1992+70dup XP_011508875.1:n.1992+70dup
NM_000393.5:c.2130+70dup MANE Select NP_000384.2:n.2130+70dup