Canonical Allele Identifier: CA2649550511
Gene: HMCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.185994774T>C , CM000663.2:g.185994774T>C GRCh38
NC_000001.10:g.185963906T>C , CM000663.1:g.185963906T>C GRCh37
NC_000001.9:g.184230529T>C NCBI36
NG_011841.1:g.265224T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000271588.9:c.3506-41T>C MANE Select ENSP00000271588.4:n.3506-41T>C
ENST00000271588.8:c.3506-41T>C ENSP00000271588.4:n.3506-41T>C
NM_031935.2:c.3506-41T>C NP_114141.2:n.3506-41T>C
XM_011510037.1:c.3506-41T>C XP_011508339.1:n.3506-41T>C
XM_011510038.1:c.3506-41T>C XP_011508340.1:n.3506-41T>C
XM_011510039.1:c.3506-41T>C XP_011508341.1:n.3506-41T>C
XM_011510040.1:c.3506-41T>C XP_011508342.1:n.3506-41T>C
XM_011510041.1:c.3506-41T>C XP_011508343.1:n.3506-41T>C
XM_011510038.3:c.3506-41T>C XP_011508340.1:n.3506-41T>C
XM_011510041.3:c.3506-41T>C XP_011508343.1:n.3506-41T>C
XM_017002437.1:c.1529-41T>C XP_016857926.1:n.1529-41T>C
XM_024450118.1:c.3506-41T>C XP_024305886.1:n.3506-41T>C
NM_031935.3:c.3506-41T>C MANE Select NP_114141.2:n.3506-41T>C