Canonical Allele Identifier: CA1315425117
Gene: COL5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1172171760
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189050837C>G , CM000664.2:g.189050837C>G GRCh38
NC_000002.11:g.189915563C>G , CM000664.1:g.189915563C>G GRCh37
NC_000002.10:g.189623808C>G NCBI36
NG_011799.1:g.134043G>C
NG_011799.2:g.134043G>C
NG_011799.3:g.179465G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.2932-161G>C MANE Select ENSP00000364000.3:n.2932-161G>C
ENST00000374866.7:c.2932-161G>C ENSP00000364000.3:n.2932-161G>C
ENST00000618828.1:c.1771-161G>C ENSP00000482184.1:n.1771-161G>C
NM_000393.3:c.2932-161G>C NP_000384.2:n.2932-161G>C
XM_011510573.1:c.2794-161G>C XP_011508875.1:n.2794-161G>C
NM_000393.4:c.2932-161G>C NP_000384.2:n.2932-161G>C
XM_011510573.3:c.2794-161G>C XP_011508875.1:n.2794-161G>C
NM_000393.5:c.2932-161G>C MANE Select NP_000384.2:n.2932-161G>C
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