Canonical Allele Identifier: CA2582720910

Gene: MAN2B1

Linked Data

• gnomAD v4: 19-12657983-A-AAAAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12657984_12657985insAAATA , CM000681.2:g.12657984_12657985insAAATA	GRCh38
NC_000019.9:g.12768798_12768799insAAATA , CM000681.1:g.12768798_12768799insAAATA	GRCh37
NC_000019.8:g.12629798_12629799insAAATA	NCBI36
NG_008318.1:g.13794_13795insATTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1309+79_1309+80insATTTT MANE Select	ENSP00000395473.2:n.1309+79_1309+80insATTTT
ENST00000221363.8:c.1306+79_1306+80insATTTT	ENSP00000221363.4:n.1306+79_1306+80insATTTT
ENST00000456935.6:c.1309+79_1309+80insATTTT	ENSP00000395473.2:n.1309+79_1309+80insATTTT
ENST00000465830.1:n.473+79_473+80insATTTT
ENST00000466794.5:n.1208+79_1208+80insATTTT
ENST00000495617.1:n.281-224_281-223insATTTT
NM_000528.3:c.1309+79_1309+80insATTTT	NP_000519.2:n.1309+79_1309+80insATTTT
NM_001173498.1:c.1306+79_1306+80insATTTT	NP_001166969.1:n.1306+79_1306+80insATTTT
XM_005259913.1:c.1312+79_1312+80insATTTT	XP_005259970.1:n.1312+79_1312+80insATTTT
XM_011528017.1:c.208+79_208+80insATTTT	XP_011526319.1:n.208+79_208+80insATTTT
XM_005259913.2:c.1312+79_1312+80insATTTT	XP_005259970.1:n.1312+79_1312+80insATTTT
XM_024451518.1:c.208+79_208+80insATTTT	XP_024307286.1:n.208+79_208+80insATTTT
NM_000528.4:c.1309+79_1309+80insATTTT MANE Select	NP_000519.2:n.1309+79_1309+80insATTTT
NM_001173498.2:c.1306+79_1306+80insATTTT	NP_001166969.1:n.1306+79_1306+80insATTTT