Canonical Allele Identifier: CA1213028297

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186174436A= , CM000663.2:g.186174436A=	GRCh38
NC_000001.10:g.186143568A= , CM000663.1:g.186143568A=	GRCh37
NC_000001.9:g.184410191A=	NCBI36
NG_011841.1:g.444886A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.15815-78A= MANE Select	ENSP00000271588.4:n.15815-78A=
ENST00000271588.8:c.15815-78A=	ENSP00000271588.4:n.15815-78A=
ENST00000414277.1:c.191-78A=	ENSP00000406205.1:n.191-78A=
NM_031935.2:c.15815-78A=	NP_114141.2:n.15815-78A=
XM_011510037.1:c.15530-78A=	XP_011508339.1:n.15530-78A=
XM_011510038.1:c.15815-78A=	XP_011508340.1:n.15815-78A=
XM_011510038.3:c.15815-78A=	XP_011508340.1:n.15815-78A=
XM_017002437.1:c.13838-78A=	XP_016857926.1:n.13838-78A=
NM_031935.3:c.15815-78A= MANE Select	NP_114141.2:n.15815-78A=