Canonical Allele Identifier: CA1315425011
Gene: COL5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189050569C= , CM000664.2:g.189050569C= GRCh38
NC_000002.11:g.189915295C= , CM000664.1:g.189915295C= GRCh37
NC_000002.10:g.189623540C= NCBI36
NG_011799.1:g.134311G=
NG_011799.2:g.134311G=
NG_011799.3:g.179733G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.3039G= MANE Select ENSP00000364000.3:p.Ala1013=
ENST00000374866.7:c.3039G= ENSP00000364000.3:p.Ala1013=
ENST00000618828.1:c.1878G= ENSP00000482184.1:p.Ala626=
NM_000393.3:c.3039G= NP_000384.2:p.Ala1013=
XM_011510573.1:c.2901G= XP_011508875.1:p.Ala967=
NM_000393.4:c.3039G= NP_000384.2:p.Ala1013=
XM_011510573.3:c.2901G= XP_011508875.1:p.Ala967=
NM_000393.5:c.3039G= MANE Select NP_000384.2:p.Ala1013=