Canonical Allele Identifier: CA2650324053
Gene: LAMB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209649918_209649919del , CM000663.2:g.209649918_209649919del GRCh38
NC_000001.10:g.209823263_209823264del , CM000663.1:g.209823263_209823264del GRCh37
NC_000001.9:g.207889886_207889887del NCBI36
NG_007116.1:g.7562_7563del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.183+50_183+51del MANE Select ENSP00000348384.3:n.183+50_183+51del
ENST00000356082.8:c.183+50_183+51del ENSP00000348384.3:n.183+50_183+51del
ENST00000367030.7:c.183+50_183+51del ENSP00000355997.3:n.183+50_183+51del
ENST00000391911.5:c.183+50_183+51del ENSP00000375778.1:n.183+50_183+51del
ENST00000415782.1:c.183+50_183+51del ENSP00000388960.1:n.183+50_183+51del
NM_000228.2:c.183+50_183+51del NP_000219.2:n.183+50_183+51del
NM_001017402.1:c.183+50_183+51del NP_001017402.1:n.183+50_183+51del
NM_001127641.1:c.183+50_183+51del NP_001121113.1:n.183+50_183+51del
XM_005273124.3:c.183+50_183+51del XP_005273181.1:n.183+50_183+51del
XM_005273124.4:c.183+50_183+51del XP_005273181.1:n.183+50_183+51del
XM_017001272.2:c.183+50_183+51del XP_016856761.1:n.183+50_183+51del
NM_000228.3:c.183+50_183+51del MANE Select NP_000219.2:n.183+50_183+51del
NM_001017402.2:c.183+50_183+51del NP_001017402.1:n.183+50_183+51del