Canonical Allele Identifier: CA2649546781
Gene: HMCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.185734640C>A , CM000663.2:g.185734640C>A GRCh38
NC_000001.10:g.185703772C>A , CM000663.1:g.185703772C>A GRCh37
NC_000001.9:g.183970395C>A NCBI36
NG_011841.1:g.5090C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271588.9:c.-140C>A MANE Select ENSP00000271588.4:n.-140C>A
ENST00000271588.8:c.-140C>A ENSP00000271588.4:n.-140C>A
NM_031935.2:c.-140C>A NP_114141.2:n.-140C>A
XM_011510037.1:c.-140C>A XP_011508339.1:n.-140C>A
XM_011510038.1:c.-140C>A XP_011508340.1:n.-140C>A
XM_011510039.1:c.-140C>A XP_011508341.1:n.-140C>A
XM_011510040.1:c.-140C>A XP_011508342.1:n.-140C>A
XM_011510041.1:c.-140C>A XP_011508343.1:n.-140C>A
XM_011510038.3:c.-140C>A XP_011508340.1:n.-140C>A
XM_011510041.3:c.-140C>A XP_011508343.1:n.-140C>A
XM_024450118.1:c.-140C>A XP_024305886.1:n.-140C>A
NM_031935.3:c.-140C>A MANE Select NP_114141.2:n.-140C>A