Canonical Allele Identifier: CA2582720911

Gene: MAN2B1

Linked Data

• gnomAD v4: 19-12657984-A-AACTC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12657984_12657985insACTC , CM000681.2:g.12657984_12657985insACTC	GRCh38
NC_000019.9:g.12768798_12768799insACTC , CM000681.1:g.12768798_12768799insACTC	GRCh37
NC_000019.8:g.12629798_12629799insACTC	NCBI36
NG_008318.1:g.13793_13794insGAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1309+78_1309+79insGAGT MANE Select	ENSP00000395473.2:n.1309+78_1309+79insGAGT
ENST00000221363.8:c.1306+78_1306+79insGAGT	ENSP00000221363.4:n.1306+78_1306+79insGAGT
ENST00000456935.6:c.1309+78_1309+79insGAGT	ENSP00000395473.2:n.1309+78_1309+79insGAGT
ENST00000465830.1:n.473+78_473+79insGAGT
ENST00000466794.5:n.1208+78_1208+79insGAGT
ENST00000495617.1:n.281-225_281-224insGAGT
NM_000528.3:c.1309+78_1309+79insGAGT	NP_000519.2:n.1309+78_1309+79insGAGT
NM_001173498.1:c.1306+78_1306+79insGAGT	NP_001166969.1:n.1306+78_1306+79insGAGT
XM_005259913.1:c.1312+78_1312+79insGAGT	XP_005259970.1:n.1312+78_1312+79insGAGT
XM_011528017.1:c.208+78_208+79insGAGT	XP_011526319.1:n.208+78_208+79insGAGT
XM_005259913.2:c.1312+78_1312+79insGAGT	XP_005259970.1:n.1312+78_1312+79insGAGT
XM_024451518.1:c.208+78_208+79insGAGT	XP_024307286.1:n.208+78_208+79insGAGT
NM_000528.4:c.1309+78_1309+79insGAGT MANE Select	NP_000519.2:n.1309+78_1309+79insGAGT
NM_001173498.2:c.1306+78_1306+79insGAGT	NP_001166969.1:n.1306+78_1306+79insGAGT