Canonical Allele Identifier: CA2650323842
Gene: LAMB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209630777_209630779del , CM000663.2:g.209630777_209630779del GRCh38
NC_000001.10:g.209804122_209804124del , CM000663.1:g.209804122_209804124del GRCh37
NC_000001.9:g.207870745_207870747del NCBI36
NG_007116.1:g.26700_26702del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.823-41_823-39del MANE Select ENSP00000348384.3:n.823-41_823-39del
ENST00000356082.8:c.823-41_823-39del ENSP00000348384.3:n.823-41_823-39del
ENST00000367030.7:c.823-41_823-39del ENSP00000355997.3:n.823-41_823-39del
ENST00000391911.5:c.823-41_823-39del ENSP00000375778.1:n.823-41_823-39del
NM_000228.2:c.823-41_823-39del NP_000219.2:n.823-41_823-39del
NM_001017402.1:c.823-41_823-39del NP_001017402.1:n.823-41_823-39del
NM_001127641.1:c.823-41_823-39del NP_001121113.1:n.823-41_823-39del
XM_005273124.3:c.823-41_823-39del XP_005273181.1:n.823-41_823-39del
XM_005273124.4:c.823-41_823-39del XP_005273181.1:n.823-41_823-39del
XM_017001272.2:c.631-41_631-39del XP_016856761.1:n.631-41_631-39del
NM_000228.3:c.823-41_823-39del MANE Select NP_000219.2:n.823-41_823-39del
NM_001017402.2:c.823-41_823-39del NP_001017402.1:n.823-41_823-39del