Canonical Allele Identifier: CA1010089027

Gene: HMCN1

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186122793dup , CM000663.2:g.186122793dup	GRCh38
NC_000001.10:g.186091925dup , CM000663.1:g.186091925dup	GRCh37
NC_000001.9:g.184358548dup	NCBI36
NG_011841.1:g.393243dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.12230-158dup MANE Select	ENSP00000271588.4:n.12230-158dup
ENST00000271588.8:c.12230-158dup	ENSP00000271588.4:n.12230-158dup
NM_031935.2:c.12230-158dup	NP_114141.2:n.12230-158dup
XM_011510037.1:c.11945-158dup	XP_011508339.1:n.11945-158dup
XM_011510038.1:c.12230-158dup	XP_011508340.1:n.12230-158dup
XM_011510039.1:c.12230-158dup	XP_011508341.1:n.12230-158dup
XM_011510038.3:c.12230-158dup	XP_011508340.1:n.12230-158dup
XM_017002437.1:c.10253-158dup	XP_016857926.1:n.10253-158dup
NM_031935.3:c.12230-158dup MANE Select	NP_114141.2:n.12230-158dup