Canonical Allele Identifier: CA2993740645
Gene: LAMB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209618457_209618462del , CM000663.2:g.209618457_209618462del GRCh38
NC_000001.10:g.209791802_209791807del , CM000663.1:g.209791802_209791807del GRCh37
NC_000001.9:g.207858425_207858430del NCBI36
NG_007116.1:g.39015_39020del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.2900_2905del MANE Select ENSP00000348384.3:p.Glu967_Glu968del
ENST00000356082.8:c.2900_2905del ENSP00000348384.3:p.Glu967_Glu968del
ENST00000367030.7:c.2900_2905del ENSP00000355997.3:p.Glu967_Glu968del
ENST00000391911.5:c.2900_2905del ENSP00000375778.1:p.Glu967_Glu968del
ENST00000455193.1:c.107_112del ENSP00000398683.1:p.Glu36_Glu37del
NM_000228.2:c.2900_2905del NP_000219.2:p.Glu967_Glu968del
NM_001017402.1:c.2900_2905del NP_001017402.1:p.Glu967_Glu968del
NM_001127641.1:c.2900_2905del NP_001121113.1:p.Glu967_Glu968del
XM_005273124.3:c.2900_2905del XP_005273181.1:p.Glu967_Glu968del
XM_005273124.4:c.2900_2905del XP_005273181.1:p.Glu967_Glu968del
XM_017001272.2:c.2708_2713del XP_016856761.1:p.Glu903_Glu904del
NM_000228.3:c.2900_2905del MANE Select NP_000219.2:p.Glu967_Glu968del
NM_001017402.2:c.2900_2905del NP_001017402.1:p.Glu967_Glu968del