Canonical Allele Identifier: CA1315422598
Gene: COL5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189035114A= , CM000664.2:g.189035114A= GRCh38
NC_000002.11:g.189899840A= , CM000664.1:g.189899840A= GRCh37
NC_000002.10:g.189608085A= NCBI36
NG_011799.1:g.149766T=
NG_011799.2:g.149766T=
NG_011799.3:g.195188T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.4155T= MANE Select ENSP00000364000.3:p.Thr1385=
ENST00000374866.7:c.4155T= ENSP00000364000.3:p.Thr1385=
ENST00000618828.1:c.2994T= ENSP00000482184.1:p.Thr998=
NM_000393.3:c.4155T= NP_000384.2:p.Thr1385=
XM_011510573.1:c.4017T= XP_011508875.1:p.Thr1339=
NM_000393.4:c.4155T= NP_000384.2:p.Thr1385=
XM_011510573.3:c.4017T= XP_011508875.1:p.Thr1339=
NM_000393.5:c.4155T= MANE Select NP_000384.2:p.Thr1385=