Canonical Allele Identifier: CA2994119068

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186171972dup , CM000663.2:g.186171972dup	GRCh38
NC_000001.10:g.186141104dup , CM000663.1:g.186141104dup	GRCh37
NC_000001.9:g.184407727dup	NCBI36
NG_011841.1:g.442422dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.15689-34dup MANE Select	ENSP00000271588.4:n.15689-34dup
ENST00000271588.8:c.15689-34dup	ENSP00000271588.4:n.15689-34dup
ENST00000414277.1:c.65-34dup	ENSP00000406205.1:n.65-34dup
ENST00000475585.1:n.277-34dup
NM_031935.2:c.15689-34dup	NP_114141.2:n.15689-34dup
XM_011510037.1:c.15404-34dup	XP_011508339.1:n.15404-34dup
XM_011510038.1:c.15689-34dup	XP_011508340.1:n.15689-34dup
XM_011510038.3:c.15689-34dup	XP_011508340.1:n.15689-34dup
XM_017002437.1:c.13712-34dup	XP_016857926.1:n.13712-34dup
NM_031935.3:c.15689-34dup MANE Select	NP_114141.2:n.15689-34dup