Canonical Allele Identifier: CA1315445917
Gene: COL5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189098755G= , CM000664.2:g.189098755G= GRCh38
NC_000002.11:g.189963481G= , CM000664.1:g.189963481G= GRCh37
NC_000002.10:g.189671726G= NCBI36
NG_011799.1:g.86125C=
NG_011799.2:g.86125C=
NG_011799.3:g.131547C=

Transcript Alleles

HGVS Amino-acid change
ENST00000374866.9:c.374C= MANE Select ENSP00000364000.3:p.Thr125=
ENST00000649966.1:c.236C= ENSP00000496785.1:p.Thr79=
ENST00000374866.7:c.374C= ENSP00000364000.3:p.Thr125=
ENST00000618828.1:c.-257C= ENSP00000482184.1:n.-257C=
NM_000393.3:c.374C= NP_000384.2:p.Thr125=
XM_011510573.1:c.236C= XP_011508875.1:p.Thr79=
NM_000393.4:c.374C= NP_000384.2:p.Thr125=
XM_011510573.3:c.236C= XP_011508875.1:p.Thr79=
NM_000393.5:c.374C= MANE Select NP_000384.2:p.Thr125=