Canonical Allele Identifier: CA2649560644
Gene: HMCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186122862A>C , CM000663.2:g.186122862A>C GRCh38
NC_000001.10:g.186091994A>C , CM000663.1:g.186091994A>C GRCh37
NC_000001.9:g.184358617A>C NCBI36
NG_011841.1:g.393312A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000271588.9:c.12230-89A>C MANE Select ENSP00000271588.4:n.12230-89A>C
ENST00000271588.8:c.12230-89A>C ENSP00000271588.4:n.12230-89A>C
NM_031935.2:c.12230-89A>C NP_114141.2:n.12230-89A>C
XM_011510037.1:c.11945-89A>C XP_011508339.1:n.11945-89A>C
XM_011510038.1:c.12230-89A>C XP_011508340.1:n.12230-89A>C
XM_011510039.1:c.12230-89A>C XP_011508341.1:n.12230-89A>C
XM_011510038.3:c.12230-89A>C XP_011508340.1:n.12230-89A>C
XM_017002437.1:c.10253-89A>C XP_016857926.1:n.10253-89A>C
NM_031935.3:c.12230-89A>C MANE Select NP_114141.2:n.12230-89A>C