Canonical Allele Identifier: CA2323505632

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12661112_12661115delinsAGCT , CM000681.2:g.12661112_12661115delinsAGCT	GRCh38
NC_000019.9:g.12771926_12771929delinsAGCT , CM000681.1:g.12771926_12771929delinsAGCT	GRCh37
NC_000019.8:g.12632926_12632929delinsAGCT	NCBI36
NG_008318.1:g.10663_10666delinsAGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1026+145_1026+148delinsAGCT MANE Select	ENSP00000395473.2:n.1026+145_1026+148delinsAGCT
ENST00000221363.8:c.1026+145_1026+148delinsAGCT	ENSP00000221363.4:n.1026+145_1026+148delinsAGCT
ENST00000456935.6:c.1026+145_1026+148delinsAGCT	ENSP00000395473.2:n.1026+145_1026+148delinsAGCT
ENST00000462144.1:n.364_367delinsAGCT
ENST00000466794.5:n.1008+145_1008+148delinsAGCT
NM_000528.3:c.1026+145_1026+148delinsAGCT	NP_000519.2:n.1026+145_1026+148delinsAGCT
NM_001173498.1:c.1026+145_1026+148delinsAGCT	NP_001166969.1:n.1026+145_1026+148delinsAGCT
XM_005259913.1:c.1026+145_1026+148delinsAGCT	XP_005259970.1:n.1026+145_1026+148delinsAGCT
XM_011528017.1:c.8+145_8+148delinsAGCT	XP_011526319.1:n.8+145_8+148delinsAGCT
XM_005259913.2:c.1026+145_1026+148delinsAGCT	XP_005259970.1:n.1026+145_1026+148delinsAGCT
XM_024451518.1:c.8+145_8+148delinsAGCT	XP_024307286.1:n.8+145_8+148delinsAGCT
NM_000528.4:c.1026+145_1026+148delinsAGCT MANE Select	NP_000519.2:n.1026+145_1026+148delinsAGCT
NM_001173498.2:c.1026+145_1026+148delinsAGCT	NP_001166969.1:n.1026+145_1026+148delinsAGCT