Canonical Allele Identifier: CA1212846585
Gene: HMCN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.185734648A>C , CM000663.2:g.185734648A>C GRCh38
NC_000001.10:g.185703780A>C , CM000663.1:g.185703780A>C GRCh37
NC_000001.9:g.183970403A>C NCBI36
NG_011841.1:g.5098A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000271588.9:c.-132A>C MANE Select ENSP00000271588.4:n.-132A>C
ENST00000271588.8:c.-132A>C ENSP00000271588.4:n.-132A>C
NM_031935.2:c.-132A>C NP_114141.2:n.-132A>C
XM_011510037.1:c.-132A>C XP_011508339.1:n.-132A>C
XM_011510038.1:c.-132A>C XP_011508340.1:n.-132A>C
XM_011510039.1:c.-132A>C XP_011508341.1:n.-132A>C
XM_011510040.1:c.-132A>C XP_011508342.1:n.-132A>C
XM_011510041.1:c.-132A>C XP_011508343.1:n.-132A>C
XM_011510038.3:c.-132A>C XP_011508340.1:n.-132A>C
XM_011510041.3:c.-132A>C XP_011508343.1:n.-132A>C
XM_024450118.1:c.-132A>C XP_024305886.1:n.-132A>C
NM_031935.3:c.-132A>C MANE Select NP_114141.2:n.-132A>C
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