Canonical Allele Identifier: CA1040409558
Gene: COL5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189058922A>T , CM000664.2:g.189058922A>T GRCh38
NC_000002.11:g.189923648A>T , CM000664.1:g.189923648A>T GRCh37
NC_000002.10:g.189631893A>T NCBI36
NG_011799.1:g.125958T>A
NG_011799.2:g.125958T>A
NG_011799.3:g.171380T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.2086-29T>A MANE Select ENSP00000364000.3:n.2086-29T>A
ENST00000374866.7:c.2086-29T>A ENSP00000364000.3:n.2086-29T>A
ENST00000470524.2:n.192-29T>A
ENST00000618828.1:c.925-29T>A ENSP00000482184.1:n.925-29T>A
NM_000393.3:c.2086-29T>A NP_000384.2:n.2086-29T>A
XM_011510573.1:c.1948-29T>A XP_011508875.1:n.1948-29T>A
NM_000393.4:c.2086-29T>A NP_000384.2:n.2086-29T>A
XM_011510573.3:c.1948-29T>A XP_011508875.1:n.1948-29T>A
NM_000393.5:c.2086-29T>A MANE Select NP_000384.2:n.2086-29T>A