Canonical Allele Identifier: CA2994114842

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186082766_186082767insG , CM000663.2:g.186082766_186082767insG	GRCh38
NC_000001.10:g.186051898_186051899insG , CM000663.1:g.186051898_186051899insG	GRCh37
NC_000001.9:g.184318521_184318522insG	NCBI36
NG_011841.1:g.353216_353217insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.8788-99_8788-98insG MANE Select	ENSP00000271588.4:n.8788-99_8788-98insG
ENST00000271588.8:c.8788-99_8788-98insG	ENSP00000271588.4:n.8788-99_8788-98insG
NM_031935.2:c.8788-99_8788-98insG	NP_114141.2:n.8788-99_8788-98insG
XM_011510037.1:c.8788-99_8788-98insG	XP_011508339.1:n.8788-99_8788-98insG
XM_011510038.1:c.8788-99_8788-98insG	XP_011508340.1:n.8788-99_8788-98insG
XM_011510039.1:c.8788-99_8788-98insG	XP_011508341.1:n.8788-99_8788-98insG
XM_011510040.1:c.8788-99_8788-98insG	XP_011508342.1:n.8788-99_8788-98insG
XM_011510041.1:c.8788-99_8788-98insG	XP_011508343.1:n.8788-99_8788-98insG
XM_011510038.3:c.8788-99_8788-98insG	XP_011508340.1:n.8788-99_8788-98insG
XM_011510041.3:c.8788-99_8788-98insG	XP_011508343.1:n.8788-99_8788-98insG
XM_017002437.1:c.6811-99_6811-98insG	XP_016857926.1:n.6811-99_6811-98insG
XM_024450118.1:c.8788-99_8788-98insG	XP_024305886.1:n.8788-99_8788-98insG
NM_031935.3:c.8788-99_8788-98insG MANE Select	NP_114141.2:n.8788-99_8788-98insG