Canonical Allele Identifier: CA2844911769

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186129962_186129963insTT , CM000663.2:g.186129962_186129963insTT	GRCh38
NC_000001.10:g.186099094_186099095insTT , CM000663.1:g.186099094_186099095insTT	GRCh37
NC_000001.9:g.184365717_184365718insTT	NCBI36
NG_011841.1:g.400412_400413insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.12905-4_12905-3insTT MANE Select	ENSP00000271588.4:n.12905-4_12905-3insTT
ENST00000271588.8:c.12905-4_12905-3insTT	ENSP00000271588.4:n.12905-4_12905-3insTT
NM_031935.2:c.12905-4_12905-3insTT	NP_114141.2:n.12905-4_12905-3insTT
XM_011510037.1:c.12620-4_12620-3insTT	XP_011508339.1:n.12620-4_12620-3insTT
XM_011510038.1:c.12905-4_12905-3insTT	XP_011508340.1:n.12905-4_12905-3insTT
XM_011510039.1:c.12905-4_12905-3insTT	XP_011508341.1:n.12905-4_12905-3insTT
XM_011510038.3:c.12905-4_12905-3insTT	XP_011508340.1:n.12905-4_12905-3insTT
XM_017002437.1:c.10928-4_10928-3insTT	XP_016857926.1:n.10928-4_10928-3insTT
NM_031935.3:c.12905-4_12905-3insTT MANE Select	NP_114141.2:n.12905-4_12905-3insTT