Canonical Allele Identifier: CA1212989866

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186082781_186082784delinsATAT , CM000663.2:g.186082781_186082784delinsATAT	GRCh38
NC_000001.10:g.186051913_186051916delinsATAT , CM000663.1:g.186051913_186051916delinsATAT	GRCh37
NC_000001.9:g.184318536_184318539delinsATAT	NCBI36
NG_011841.1:g.353231_353234delinsATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.8788-84_8788-81delinsATAT MANE Select	ENSP00000271588.4:n.8788-84_8788-81delinsATAT
ENST00000271588.8:c.8788-84_8788-81delinsATAT	ENSP00000271588.4:n.8788-84_8788-81delinsATAT
NM_031935.2:c.8788-84_8788-81delinsATAT	NP_114141.2:n.8788-84_8788-81delinsATAT
XM_011510037.1:c.8788-84_8788-81delinsATAT	XP_011508339.1:n.8788-84_8788-81delinsATAT
XM_011510038.1:c.8788-84_8788-81delinsATAT	XP_011508340.1:n.8788-84_8788-81delinsATAT
XM_011510039.1:c.8788-84_8788-81delinsATAT	XP_011508341.1:n.8788-84_8788-81delinsATAT
XM_011510040.1:c.8788-84_8788-81delinsATAT	XP_011508342.1:n.8788-84_8788-81delinsATAT
XM_011510041.1:c.8788-84_8788-81delinsATAT	XP_011508343.1:n.8788-84_8788-81delinsATAT
XM_011510038.3:c.8788-84_8788-81delinsATAT	XP_011508340.1:n.8788-84_8788-81delinsATAT
XM_011510041.3:c.8788-84_8788-81delinsATAT	XP_011508343.1:n.8788-84_8788-81delinsATAT
XM_017002437.1:c.6811-84_6811-81delinsATAT	XP_016857926.1:n.6811-84_6811-81delinsATAT
XM_024450118.1:c.8788-84_8788-81delinsATAT	XP_024305886.1:n.8788-84_8788-81delinsATAT
NM_031935.3:c.8788-84_8788-81delinsATAT MANE Select	NP_114141.2:n.8788-84_8788-81delinsATAT