Canonical Allele Identifier: CA1315425113
Gene: COL5A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189050828A= , CM000664.2:g.189050828A= GRCh38
NC_000002.11:g.189915554A= , CM000664.1:g.189915554A= GRCh37
NC_000002.10:g.189623799A= NCBI36
NG_011799.1:g.134052T=
NG_011799.2:g.134052T=
NG_011799.3:g.179474T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.2932-152T= MANE Select ENSP00000364000.3:n.2932-152T=
ENST00000374866.7:c.2932-152T= ENSP00000364000.3:n.2932-152T=
ENST00000618828.1:c.1771-152T= ENSP00000482184.1:n.1771-152T=
NM_000393.3:c.2932-152T= NP_000384.2:n.2932-152T=
XM_011510573.1:c.2794-152T= XP_011508875.1:n.2794-152T=
NM_000393.4:c.2932-152T= NP_000384.2:n.2932-152T=
XM_011510573.3:c.2794-152T= XP_011508875.1:n.2794-152T=
NM_000393.5:c.2932-152T= MANE Select NP_000384.2:n.2932-152T=
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