This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: CA1213006355
Gene: HMCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186122796_186122797delinsTC , CM000663.2:g.186122796_186122797delinsTC GRCh38
NC_000001.10:g.186091928_186091929delinsTC , CM000663.1:g.186091928_186091929delinsTC GRCh37
NC_000001.9:g.184358551_184358552delinsTC NCBI36
NG_011841.1:g.393246_393247delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000271588.9:c.12230-155_12230-154delinsTC MANE Select ENSP00000271588.4:n.12230-155_12230-154delinsTC
ENST00000271588.8:c.12230-155_12230-154delinsTC ENSP00000271588.4:n.12230-155_12230-154delinsTC
NM_031935.2:c.12230-155_12230-154delinsTC NP_114141.2:n.12230-155_12230-154delinsTC
XM_011510037.1:c.11945-155_11945-154delinsTC XP_011508339.1:n.11945-155_11945-154delinsTC
XM_011510038.1:c.12230-155_12230-154delinsTC XP_011508340.1:n.12230-155_12230-154delinsTC
XM_011510039.1:c.12230-155_12230-154delinsTC XP_011508341.1:n.12230-155_12230-154delinsTC
XM_011510038.3:c.12230-155_12230-154delinsTC XP_011508340.1:n.12230-155_12230-154delinsTC
XM_017002437.1:c.10253-155_10253-154delinsTC XP_016857926.1:n.10253-155_10253-154delinsTC
NM_031935.3:c.12230-155_12230-154delinsTC MANE Select NP_114141.2:n.12230-155_12230-154delinsTC