Canonical Allele Identifier: CA2649561985

Gene: HMCN1

Linked Data

• gnomAD v4: 1-186174451-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186174451_186174452insC , CM000663.2:g.186174451_186174452insC	GRCh38
NC_000001.10:g.186143583_186143584insC , CM000663.1:g.186143583_186143584insC	GRCh37
NC_000001.9:g.184410206_184410207insC	NCBI36
NG_011841.1:g.444901_444902insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.15815-63_15815-62insC MANE Select	ENSP00000271588.4:n.15815-63_15815-62insC
ENST00000271588.8:c.15815-63_15815-62insC	ENSP00000271588.4:n.15815-63_15815-62insC
ENST00000414277.1:c.191-63_191-62insC	ENSP00000406205.1:n.191-63_191-62insC
NM_031935.2:c.15815-63_15815-62insC	NP_114141.2:n.15815-63_15815-62insC
XM_011510037.1:c.15530-63_15530-62insC	XP_011508339.1:n.15530-63_15530-62insC
XM_011510038.1:c.15815-63_15815-62insC	XP_011508340.1:n.15815-63_15815-62insC
XM_011510038.3:c.15815-63_15815-62insC	XP_011508340.1:n.15815-63_15815-62insC
XM_017002437.1:c.13838-63_13838-62insC	XP_016857926.1:n.13838-63_13838-62insC
NM_031935.3:c.15815-63_15815-62insC MANE Select	NP_114141.2:n.15815-63_15815-62insC