Canonical Allele Identifier: CA343885977
Gene: HMCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186015392A>T , CM000663.2:g.186015392A>T GRCh38
NC_000001.10:g.185984524A>T , CM000663.1:g.185984524A>T GRCh37
NC_000001.9:g.184251147A>T NCBI36
NG_011841.1:g.285842A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000271588.9:c.4864A>T MANE Select ENSP00000271588.4:p.Asn1622Tyr
ENST00000271588.8:c.4864A>T ENSP00000271588.4:p.Asn1622Tyr
NM_031935.2:c.4864A>T NP_114141.2:p.Asn1622Tyr
XM_011510037.1:c.4864A>T XP_011508339.1:p.Asn1622Tyr
XM_011510038.1:c.4864A>T XP_011508340.1:p.Asn1622Tyr
XM_011510039.1:c.4864A>T XP_011508341.1:p.Asn1622Tyr
XM_011510040.1:c.4864A>T XP_011508342.1:p.Asn1622Tyr
XM_011510041.1:c.4864A>T XP_011508343.1:p.Asn1622Tyr
XM_011510038.3:c.4864A>T XP_011508340.1:p.Asn1622Tyr
XM_011510041.3:c.4864A>T XP_011508343.1:p.Asn1622Tyr
XM_017002437.1:c.2887A>T XP_016857926.1:p.Asn963Tyr
XM_024450118.1:c.4864A>T XP_024305886.1:p.Asn1622Tyr
NM_031935.3:c.4864A>T MANE Select NP_114141.2:p.Asn1622Tyr