Canonical Allele Identifier: CA2323506689

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12663306_12663307delinsAC , CM000681.2:g.12663306_12663307delinsAC	GRCh38
NC_000019.9:g.12774120_12774121delinsAC , CM000681.1:g.12774120_12774121delinsAC	GRCh37
NC_000019.8:g.12635120_12635121delinsAC	NCBI36
NG_008318.1:g.8471_8472delinsGT
NG_015814.1:g.1503_1504delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.909+10_909+11delinsGT MANE Select	ENSP00000395473.2:n.909+10_909+11delinsGT...
ENST00000221363.8:c.909+10_909+11delinsGT	ENSP00000221363.4:n.909+10_909+11delinsGT...
ENST00000456935.6:c.909+10_909+11delinsGT	ENSP00000395473.2:n.909+10_909+11delinsGT...
ENST00000462144.1:n.102+10_102+11delinsGT
ENST00000466794.5:n.891+10_891+11delinsGT
NM_000528.3:c.909+10_909+11delinsGT	NP_000519.2:n.909+10_909+11delinsGT
NM_001173498.1:c.909+10_909+11delinsGT	NP_001166969.1:n.909+10_909+11delinsGT
XM_005259913.1:c.909+10_909+11delinsGT	XP_005259970.1:n.909+10_909+11delinsGT
XM_011528017.1:c.-110+10_-110+11delinsGT	XP_011526319.1:n.-110+10_-110+11delinsGT
XM_005259913.2:c.909+10_909+11delinsGT	XP_005259970.1:n.909+10_909+11delinsGT
XM_024451518.1:c.-110+10_-110+11delinsGT	XP_024307286.1:n.-110+10_-110+11delinsGT
NM_000528.4:c.909+10_909+11delinsGT MANE Select	NP_000519.2:n.909+10_909+11delinsGT
NM_001173498.2:c.909+10_909+11delinsGT	NP_001166969.1:n.909+10_909+11delinsGT