Canonical Allele Identifier: CA1144655665

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186129950_186129954delinsTTCTT , CM000663.2:g.186129950_186129954delinsTTCTT	GRCh38
NC_000001.10:g.186099082_186099086delinsTTCTT , CM000663.1:g.186099082_186099086delinsTTCTT	GRCh37
NC_000001.9:g.184365705_184365709delinsTTCTT	NCBI36
NG_011841.1:g.400400_400404delinsTTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.12905-16_12905-12delinsTTCTT MANE Select	ENSP00000271588.4:n.12905-16_12905-12delinsTTCTT
ENST00000271588.8:c.12905-16_12905-12delinsTTCTT	ENSP00000271588.4:n.12905-16_12905-12delinsTTCTT
NM_031935.2:c.12905-16_12905-12delinsTTCTT	NP_114141.2:n.12905-16_12905-12delinsTTCTT
XM_011510037.1:c.12620-16_12620-12delinsTTCTT	XP_011508339.1:n.12620-16_12620-12delinsTTCTT
XM_011510038.1:c.12905-16_12905-12delinsTTCTT	XP_011508340.1:n.12905-16_12905-12delinsTTCTT
XM_011510039.1:c.12905-16_12905-12delinsTTCTT	XP_011508341.1:n.12905-16_12905-12delinsTTCTT
XM_011510038.3:c.12905-16_12905-12delinsTTCTT	XP_011508340.1:n.12905-16_12905-12delinsTTCTT
XM_017002437.1:c.10928-16_10928-12delinsTTCTT	XP_016857926.1:n.10928-16_10928-12delinsTTCTT
NM_031935.3:c.12905-16_12905-12delinsTTCTT MANE Select	NP_114141.2:n.12905-16_12905-12delinsTTCTT