Canonical Allele Identifier: CA1315428697
Gene: COL5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189059295C= , CM000664.2:g.189059295C= GRCh38
NC_000002.11:g.189924021C= , CM000664.1:g.189924021C= GRCh37
NC_000002.10:g.189632266C= NCBI36
NG_011799.1:g.125585G=
NG_011799.2:g.125585G=
NG_011799.3:g.171007G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.2086-402G= MANE Select ENSP00000364000.3:n.2086-402G=
ENST00000374866.7:c.2086-402G= ENSP00000364000.3:n.2086-402G=
ENST00000470524.2:n.192-402G=
ENST00000618828.1:c.925-402G= ENSP00000482184.1:n.925-402G=
NM_000393.3:c.2086-402G= NP_000384.2:n.2086-402G=
XM_011510573.1:c.1948-402G= XP_011508875.1:n.1948-402G=
NM_000393.4:c.2086-402G= NP_000384.2:n.2086-402G=
XM_011510573.3:c.1948-402G= XP_011508875.1:n.1948-402G=
NM_000393.5:c.2086-402G= MANE Select NP_000384.2:n.2086-402G=