Canonical Allele Identifier: CA2649561879

Gene: HMCN1

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186172057del , CM000663.2:g.186172057del	GRCh38
NC_000001.10:g.186141189del , CM000663.1:g.186141189del	GRCh37
NC_000001.9:g.184407812del	NCBI36
NG_011841.1:g.442507del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.15740del MANE Select	ENSP00000271588.4:p.Asn5247ThrfsTer16
ENST00000271588.8:c.15740del	ENSP00000271588.4:p.Asn5247ThrfsTer16
ENST00000414277.1:c.116del	ENSP00000406205.1:p.Asn39ThrfsTer16
ENST00000475585.1:n.328del
NM_031935.2:c.15740del	NP_114141.2:p.Asn5247ThrfsTer16
XM_011510037.1:c.15455del	XP_011508339.1:p.Asn5152ThrfsTer16
XM_011510038.1:c.15740del	XP_011508340.1:p.Asn5247ThrfsTer16
XM_011510038.3:c.15740del	XP_011508340.1:p.Asn5247ThrfsTer16
XM_017002437.1:c.13763del	XP_016857926.1:p.Asn4588ThrfsTer16
NM_031935.3:c.15740del MANE Select	NP_114141.2:p.Asn5247ThrfsTer16