Canonical Allele Identifier: CA1213027218

Gene: HMCN1

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186171965_186171968del , CM000663.2:g.186171965_186171968del	GRCh38
NC_000001.10:g.186141097_186141100del , CM000663.1:g.186141097_186141100del	GRCh37
NC_000001.9:g.184407720_184407723del	NCBI36
NG_011841.1:g.442415_442418del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.15689-41_15689-38del MANE Select	ENSP00000271588.4:n.15689-41_15689-38del
ENST00000271588.8:c.15689-41_15689-38del	ENSP00000271588.4:n.15689-41_15689-38del
ENST00000414277.1:c.65-41_65-38del	ENSP00000406205.1:n.65-41_65-38del
ENST00000475585.1:n.277-41_277-38del
NM_031935.2:c.15689-41_15689-38del	NP_114141.2:n.15689-41_15689-38del
XM_011510037.1:c.15404-41_15404-38del	XP_011508339.1:n.15404-41_15404-38del
XM_011510038.1:c.15689-41_15689-38del	XP_011508340.1:n.15689-41_15689-38del
XM_011510038.3:c.15689-41_15689-38del	XP_011508340.1:n.15689-41_15689-38del
XM_017002437.1:c.13712-41_13712-38del	XP_016857926.1:n.13712-41_13712-38del
NM_031935.3:c.15689-41_15689-38del MANE Select	NP_114141.2:n.15689-41_15689-38del