Canonical Allele Identifier: CA2580096558
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1899854
ClinVar RCV Id: RCV002575683

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12663394_12663395delinsCT , CM000681.2:g.12663394_12663395delinsCT GRCh38
NC_000019.9:g.12774208_12774209delinsCT , CM000681.1:g.12774208_12774209delinsCT GRCh37
NC_000019.8:g.12635208_12635209delinsCT NCBI36
NG_008318.1:g.8383_8384delinsAG
NG_015814.1:g.1591_1592delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000456935.7:c.831_832delinsAG MANE Select ENSP00000395473.2:p.Leu278Val
ENST00000221363.8:c.831_832delinsAG ENSP00000221363.4:p.Leu278Val
ENST00000456935.6:c.831_832delinsAG ENSP00000395473.2:p.Leu278Val
ENST00000462144.1:n.24_25delinsAG
ENST00000466794.5:n.813_814delinsAG
NM_000528.3:c.831_832delinsAG NP_000519.2:p.Leu278Val
NM_001173498.1:c.831_832delinsAG NP_001166969.1:p.Leu278Val
XM_005259913.1:c.831_832delinsAG XP_005259970.1:p.Leu278Val
XM_005259913.2:c.831_832delinsAG XP_005259970.1:p.Leu278Val
XM_024451518.1:c.-188_-187delinsAG XP_024307286.1:n.-188_-187delinsAG
NM_000528.4:c.831_832delinsAG MANE Select NP_000519.2:p.Leu278Val
NM_001173498.2:c.831_832delinsAG NP_001166969.1:p.Leu278Val