Canonical Allele Identifier: CA1315445886
Gene: COL5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189098682T= , CM000664.2:g.189098682T= GRCh38
NC_000002.11:g.189963408T= , CM000664.1:g.189963408T= GRCh37
NC_000002.10:g.189671653T= NCBI36
NG_011799.1:g.86198A=
NG_011799.2:g.86198A=
NG_011799.3:g.131620A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.402+45A= MANE Select ENSP00000364000.3:n.402+45A=
ENST00000649966.1:c.264+45A= ENSP00000496785.1:n.264+45A=
ENST00000374866.7:c.402+45A= ENSP00000364000.3:n.402+45A=
ENST00000618828.1:c.-229+45A= ENSP00000482184.1:n.-229+45A=
NM_000393.3:c.402+45A= NP_000384.2:n.402+45A=
XM_011510573.1:c.264+45A= XP_011508875.1:n.264+45A=
NM_000393.4:c.402+45A= NP_000384.2:n.402+45A=
XM_011510573.3:c.264+45A= XP_011508875.1:n.264+45A=
NM_000393.5:c.402+45A= MANE Select NP_000384.2:n.402+45A=