Canonical Allele Identifier: CA1144056080

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186174430_186174431delinsAA , CM000663.2:g.186174430_186174431delinsAA	GRCh38
NC_000001.10:g.186143562_186143563delinsAA , CM000663.1:g.186143562_186143563delinsAA	GRCh37
NC_000001.9:g.184410185_184410186delinsAA	NCBI36
NG_011841.1:g.444880_444881delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.15815-84_15815-83delinsAA MANE Select	ENSP00000271588.4:n.15815-84_15815-83delinsAA
ENST00000271588.8:c.15815-84_15815-83delinsAA	ENSP00000271588.4:n.15815-84_15815-83delinsAA
ENST00000414277.1:c.191-84_191-83delinsAA	ENSP00000406205.1:n.191-84_191-83delinsAA
NM_031935.2:c.15815-84_15815-83delinsAA	NP_114141.2:n.15815-84_15815-83delinsAA
XM_011510037.1:c.15530-84_15530-83delinsAA	XP_011508339.1:n.15530-84_15530-83delinsAA
XM_011510038.1:c.15815-84_15815-83delinsAA	XP_011508340.1:n.15815-84_15815-83delinsAA
XM_011510038.3:c.15815-84_15815-83delinsAA	XP_011508340.1:n.15815-84_15815-83delinsAA
XM_017002437.1:c.13838-84_13838-83delinsAA	XP_016857926.1:n.13838-84_13838-83delinsAA
NM_031935.3:c.15815-84_15815-83delinsAA MANE Select	NP_114141.2:n.15815-84_15815-83delinsAA