Canonical Allele Identifier: CA1315445891
Gene: COL5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189098689A= , CM000664.2:g.189098689A= GRCh38
NC_000002.11:g.189963415A= , CM000664.1:g.189963415A= GRCh37
NC_000002.10:g.189671660A= NCBI36
NG_011799.1:g.86191T=
NG_011799.2:g.86191T=
NG_011799.3:g.131613T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.402+38T= MANE Select ENSP00000364000.3:n.402+38T=
ENST00000649966.1:c.264+38T= ENSP00000496785.1:n.264+38T=
ENST00000374866.7:c.402+38T= ENSP00000364000.3:n.402+38T=
ENST00000618828.1:c.-229+38T= ENSP00000482184.1:n.-229+38T=
NM_000393.3:c.402+38T= NP_000384.2:n.402+38T=
XM_011510573.1:c.264+38T= XP_011508875.1:n.264+38T=
NM_000393.4:c.402+38T= NP_000384.2:n.402+38T=
XM_011510573.3:c.264+38T= XP_011508875.1:n.264+38T=
NM_000393.5:c.402+38T= MANE Select NP_000384.2:n.402+38T=