Canonical Allele Identifier: CA2580065363
Gene: COL5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2057593
ClinVar RCV Id: RCV002923438
gnomAD v4: 2-189062935-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189062935A>G , CM000664.2:g.189062935A>G GRCh38
NC_000002.11:g.189927661A>G , CM000664.1:g.189927661A>G GRCh37
NC_000002.10:g.189635906A>G NCBI36
NG_011799.1:g.121945T>C
NG_011799.2:g.121945T>C
NG_011799.3:g.167367T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.1924-17T>C MANE Select ENSP00000364000.3:n.1924-17T>C
ENST00000374866.7:c.1924-17T>C ENSP00000364000.3:n.1924-17T>C
ENST00000470524.2:n.30-17T>C
ENST00000618828.1:c.763-17T>C ENSP00000482184.1:n.763-17T>C
NM_000393.3:c.1924-17T>C NP_000384.2:n.1924-17T>C
XM_011510573.1:c.1786-17T>C XP_011508875.1:n.1786-17T>C
NM_000393.4:c.1924-17T>C NP_000384.2:n.1924-17T>C
XM_011510573.3:c.1786-17T>C XP_011508875.1:n.1786-17T>C
NM_000393.5:c.1924-17T>C MANE Select NP_000384.2:n.1924-17T>C
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