Canonical Allele Identifier: CA1213028299

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186174447_186174448delinsAC , CM000663.2:g.186174447_186174448delinsAC	GRCh38
NC_000001.10:g.186143579_186143580delinsAC , CM000663.1:g.186143579_186143580delinsAC	GRCh37
NC_000001.9:g.184410202_184410203delinsAC	NCBI36
NG_011841.1:g.444897_444898delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.15815-67_15815-66delinsAC MANE Select	ENSP00000271588.4:n.15815-67_15815-66delinsAC
ENST00000271588.8:c.15815-67_15815-66delinsAC	ENSP00000271588.4:n.15815-67_15815-66delinsAC
ENST00000414277.1:c.191-67_191-66delinsAC	ENSP00000406205.1:n.191-67_191-66delinsAC
NM_031935.2:c.15815-67_15815-66delinsAC	NP_114141.2:n.15815-67_15815-66delinsAC
XM_011510037.1:c.15530-67_15530-66delinsAC	XP_011508339.1:n.15530-67_15530-66delinsAC
XM_011510038.1:c.15815-67_15815-66delinsAC	XP_011508340.1:n.15815-67_15815-66delinsAC
XM_011510038.3:c.15815-67_15815-66delinsAC	XP_011508340.1:n.15815-67_15815-66delinsAC
XM_017002437.1:c.13838-67_13838-66delinsAC	XP_016857926.1:n.13838-67_13838-66delinsAC
NM_031935.3:c.15815-67_15815-66delinsAC MANE Select	NP_114141.2:n.15815-67_15815-66delinsAC