Canonical Allele Identifier: CA1315425027
Gene: COL5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189050607G= , CM000664.2:g.189050607G= GRCh38
NC_000002.11:g.189915333G= , CM000664.1:g.189915333G= GRCh37
NC_000002.10:g.189623578G= NCBI36
NG_011799.1:g.134273C=
NG_011799.2:g.134273C=
NG_011799.3:g.179695C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.3001C= MANE Select ENSP00000364000.3:p.Arg1001=
ENST00000374866.7:c.3001C= ENSP00000364000.3:p.Arg1001=
ENST00000618828.1:c.1840C= ENSP00000482184.1:p.Arg614=
NM_000393.3:c.3001C= NP_000384.2:p.Arg1001=
XM_011510573.1:c.2863C= XP_011508875.1:p.Arg955=
NM_000393.4:c.3001C= NP_000384.2:p.Arg1001=
XM_011510573.3:c.2863C= XP_011508875.1:p.Arg955=
NM_000393.5:c.3001C= MANE Select NP_000384.2:p.Arg1001=