Canonical Allele Identifier: CA2650319108
Gene: LAMB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209615072_209615075del , CM000663.2:g.209615072_209615075del GRCh38
NC_000001.10:g.209788417_209788420del , CM000663.1:g.209788417_209788420del GRCh37
NC_000001.9:g.207855040_207855043del NCBI36
NG_007116.1:g.42405_42408del

Transcript Alleles

HGVS Amino-acid change
ENST00000356082.9:c.*200_*203del MANE Select ENSP00000348384.3:n.*200_*203del
ENST00000356082.8:c.*200_*203del ENSP00000348384.3:n.*200_*203del
ENST00000367030.7:c.*200_*203del ENSP00000355997.3:n.*200_*203del
ENST00000391911.5:c.*200_*203del ENSP00000375778.1:n.*200_*203del
NM_000228.2:c.*200_*203del NP_000219.2:n.*200_*203del
NM_001017402.1:c.*200_*203del NP_001017402.1:n.*200_*203del
NM_001127641.1:c.*200_*203del NP_001121113.1:n.*200_*203del
XM_005273124.3:c.*200_*203del XP_005273181.1:n.*200_*203del
XM_005273124.4:c.*200_*203del XP_005273181.1:n.*200_*203del
XM_017001272.2:c.*200_*203del XP_016856761.1:n.*200_*203del
NM_000228.3:c.*200_*203del MANE Select NP_000219.2:n.*200_*203del
NM_001017402.2:c.*200_*203del NP_001017402.1:n.*200_*203del