Canonical Allele Identifier: CA2844911766

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186129951_186129952insTCTAC , CM000663.2:g.186129951_186129952insTCTAC	GRCh38
NC_000001.10:g.186099083_186099084insTCTAC , CM000663.1:g.186099083_186099084insTCTAC	GRCh37
NC_000001.9:g.184365706_184365707insTCTAC	NCBI36
NG_011841.1:g.400401_400402insTCTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.12905-15_12905-14insTCTAC MANE Select	ENSP00000271588.4:n.12905-15_12905-14insTCTAC
ENST00000271588.8:c.12905-15_12905-14insTCTAC	ENSP00000271588.4:n.12905-15_12905-14insTCTAC
NM_031935.2:c.12905-15_12905-14insTCTAC	NP_114141.2:n.12905-15_12905-14insTCTAC
XM_011510037.1:c.12620-15_12620-14insTCTAC	XP_011508339.1:n.12620-15_12620-14insTCTAC
XM_011510038.1:c.12905-15_12905-14insTCTAC	XP_011508340.1:n.12905-15_12905-14insTCTAC
XM_011510039.1:c.12905-15_12905-14insTCTAC	XP_011508341.1:n.12905-15_12905-14insTCTAC
XM_011510038.3:c.12905-15_12905-14insTCTAC	XP_011508340.1:n.12905-15_12905-14insTCTAC
XM_017002437.1:c.10928-15_10928-14insTCTAC	XP_016857926.1:n.10928-15_10928-14insTCTAC
NM_031935.3:c.12905-15_12905-14insTCTAC MANE Select	NP_114141.2:n.12905-15_12905-14insTCTAC