Canonical Allele Identifier: CA2649555644

Gene: HMCN1

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186082781_186082787del , CM000663.2:g.186082781_186082787del	GRCh38
NC_000001.10:g.186051913_186051919del , CM000663.1:g.186051913_186051919del	GRCh37
NC_000001.9:g.184318536_184318542del	NCBI36
NG_011841.1:g.353231_353237del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.8788-84_8788-78del MANE Select	ENSP00000271588.4:n.8788-84_8788-78del
ENST00000271588.8:c.8788-84_8788-78del	ENSP00000271588.4:n.8788-84_8788-78del
NM_031935.2:c.8788-84_8788-78del	NP_114141.2:n.8788-84_8788-78del
XM_011510037.1:c.8788-84_8788-78del	XP_011508339.1:n.8788-84_8788-78del
XM_011510038.1:c.8788-84_8788-78del	XP_011508340.1:n.8788-84_8788-78del
XM_011510039.1:c.8788-84_8788-78del	XP_011508341.1:n.8788-84_8788-78del
XM_011510040.1:c.8788-84_8788-78del	XP_011508342.1:n.8788-84_8788-78del
XM_011510041.1:c.8788-84_8788-78del	XP_011508343.1:n.8788-84_8788-78del
XM_011510038.3:c.8788-84_8788-78del	XP_011508340.1:n.8788-84_8788-78del
XM_011510041.3:c.8788-84_8788-78del	XP_011508343.1:n.8788-84_8788-78del
XM_017002437.1:c.6811-84_6811-78del	XP_016857926.1:n.6811-84_6811-78del
XM_024450118.1:c.8788-84_8788-78del	XP_024305886.1:n.8788-84_8788-78del
NM_031935.3:c.8788-84_8788-78del MANE Select	NP_114141.2:n.8788-84_8788-78del