Canonical Allele Identifier: CA2582721586

Gene: MAN2B1

Linked Data

• gnomAD v4: 19-12660941-TAGAGAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12660944_12660949del , CM000681.2:g.12660944_12660949del	GRCh38
NC_000019.9:g.12771758_12771763del , CM000681.1:g.12771758_12771763del	GRCh37
NC_000019.8:g.12632758_12632763del	NCBI36
NG_008318.1:g.10831_10836del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1026+313_1026+318del MANE Select	ENSP00000395473.2:n.1026+313_1026+318del
ENST00000221363.8:c.1026+313_1026+318del	ENSP00000221363.4:n.1026+313_1026+318del
ENST00000456935.6:c.1026+313_1026+318del	ENSP00000395473.2:n.1026+313_1026+318del
ENST00000462144.1:n.532_537del
ENST00000466794.5:n.1008+313_1008+318del
NM_000528.3:c.1026+313_1026+318del	NP_000519.2:n.1026+313_1026+318del
NM_001173498.1:c.1026+313_1026+318del	NP_001166969.1:n.1026+313_1026+318del
XM_005259913.1:c.1026+313_1026+318del	XP_005259970.1:n.1026+313_1026+318del
XM_011528017.1:c.8+313_8+318del	XP_011526319.1:n.8+313_8+318del
XM_005259913.2:c.1026+313_1026+318del	XP_005259970.1:n.1026+313_1026+318del
XM_024451518.1:c.8+313_8+318del	XP_024307286.1:n.8+313_8+318del
NM_000528.4:c.1026+313_1026+318del MANE Select	NP_000519.2:n.1026+313_1026+318del
NM_001173498.2:c.1026+313_1026+318del	NP_001166969.1:n.1026+313_1026+318del