Canonical Allele Identifier: CA1315428499
Gene: COL5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189058757T= , CM000664.2:g.189058757T= GRCh38
NC_000002.11:g.189923483T= , CM000664.1:g.189923483T= GRCh37
NC_000002.10:g.189631728T= NCBI36
NG_011799.1:g.126123A=
NG_011799.2:g.126123A=
NG_011799.3:g.171545A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.2130+92A= MANE Select ENSP00000364000.3:n.2130+92A=
ENST00000374866.7:c.2130+92A= ENSP00000364000.3:n.2130+92A=
ENST00000470524.2:n.236+92A=
ENST00000618828.1:c.969+92A= ENSP00000482184.1:n.969+92A=
NM_000393.3:c.2130+92A= NP_000384.2:n.2130+92A=
XM_011510573.1:c.1992+92A= XP_011508875.1:n.1992+92A=
NM_000393.4:c.2130+92A= NP_000384.2:n.2130+92A=
XM_011510573.3:c.1992+92A= XP_011508875.1:n.1992+92A=
NM_000393.5:c.2130+92A= MANE Select NP_000384.2:n.2130+92A=