Canonical Allele Identifier: CA1213006469

Gene: HMCN1

Linked Data

• dbSNP Id: rs1661464893

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186122944_186122947dup , CM000663.2:g.186122944_186122947dup	GRCh38
NC_000001.10:g.186092076_186092079dup , CM000663.1:g.186092076_186092079dup	GRCh37
NC_000001.9:g.184358699_184358702dup	NCBI36
NG_011841.1:g.393394_393397dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.12230-7_12230-4dup MANE Select	ENSP00000271588.4:n.12230-7_12230-4dup
ENST00000271588.8:c.12230-7_12230-4dup	ENSP00000271588.4:n.12230-7_12230-4dup
NM_031935.2:c.12230-7_12230-4dup	NP_114141.2:n.12230-7_12230-4dup
XM_011510037.1:c.11945-7_11945-4dup	XP_011508339.1:n.11945-7_11945-4dup
XM_011510038.1:c.12230-7_12230-4dup	XP_011508340.1:n.12230-7_12230-4dup
XM_011510039.1:c.12230-7_12230-4dup	XP_011508341.1:n.12230-7_12230-4dup
XM_011510038.3:c.12230-7_12230-4dup	XP_011508340.1:n.12230-7_12230-4dup
XM_017002437.1:c.10253-7_10253-4dup	XP_016857926.1:n.10253-7_10253-4dup
NM_031935.3:c.12230-7_12230-4dup MANE Select	NP_114141.2:n.12230-7_12230-4dup