Canonical Allele Identifier: CA1212950878

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.185993136_185993137delinsTA , CM000663.2:g.185993136_185993137delinsTA	GRCh38
NC_000001.10:g.185962268_185962269delinsTA , CM000663.1:g.185962268_185962269delinsTA	GRCh37
NC_000001.9:g.184228891_184228892delinsTA	NCBI36
NG_011841.1:g.263586_263587delinsTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000271588.9:c.3378-46_3378-45delinsTA MANE Select	ENSP00000271588.4:n.3378-46_3378-45delins...
ENST00000271588.8:c.3378-46_3378-45delinsTA	ENSP00000271588.4:n.3378-46_3378-45delins...
ENST00000485744.5:n.1629-46_1629-45delinsTA
NM_031935.2:c.3378-46_3378-45delinsTA	NP_114141.2:n.3378-46_3378-45delinsTA
XM_011510037.1:c.3378-46_3378-45delinsTA	XP_011508339.1:n.3378-46_3378-45delinsTA
XM_011510038.1:c.3378-46_3378-45delinsTA	XP_011508340.1:n.3378-46_3378-45delinsTA
XM_011510039.1:c.3378-46_3378-45delinsTA	XP_011508341.1:n.3378-46_3378-45delinsTA
XM_011510040.1:c.3378-46_3378-45delinsTA	XP_011508342.1:n.3378-46_3378-45delinsTA
XM_011510041.1:c.3378-46_3378-45delinsTA	XP_011508343.1:n.3378-46_3378-45delinsTA
XM_011510038.3:c.3378-46_3378-45delinsTA	XP_011508340.1:n.3378-46_3378-45delinsTA
XM_011510041.3:c.3378-46_3378-45delinsTA	XP_011508343.1:n.3378-46_3378-45delinsTA
XM_017002437.1:c.1401-46_1401-45delinsTA	XP_016857926.1:n.1401-46_1401-45delinsTA
XM_024450118.1:c.3378-46_3378-45delinsTA	XP_024305886.1:n.3378-46_3378-45delinsTA
NM_031935.3:c.3378-46_3378-45delinsTA MANE Select	NP_114141.2:n.3378-46_3378-45delinsTA