Canonical Allele Identifier: CA1315418796
Gene: COL5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189045849G= , CM000664.2:g.189045849G= GRCh38
NC_000002.11:g.189910575G= , CM000664.1:g.189910575G= GRCh37
NC_000002.10:g.189618820G= NCBI36
NG_011799.1:g.139031C=
NG_011799.2:g.139031C=
NG_011799.3:g.184453C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.3260C= MANE Select ENSP00000364000.3:p.Thr1087=
ENST00000374866.7:c.3260C= ENSP00000364000.3:p.Thr1087=
ENST00000618828.1:c.2099C= ENSP00000482184.1:p.Thr700=
NM_000393.3:c.3260C= NP_000384.2:p.Thr1087=
XM_011510573.1:c.3122C= XP_011508875.1:p.Thr1041=
NM_000393.4:c.3260C= NP_000384.2:p.Thr1087=
XM_011510573.3:c.3122C= XP_011508875.1:p.Thr1041=
NM_000393.5:c.3260C= MANE Select NP_000384.2:p.Thr1087=