Canonical Allele Identifier: CA2650322168
Gene: LAMB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209632735_209632737del , CM000663.2:g.209632735_209632737del GRCh38
NC_000001.10:g.209806080_209806082del , CM000663.1:g.209806080_209806082del GRCh37
NC_000001.9:g.207872703_207872705del NCBI36
NG_007116.1:g.24739_24741del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.668_670del MANE Select ENSP00000348384.3:p.Arg223_Leu224delinsMet
ENST00000356082.8:c.668_670del ENSP00000348384.3:p.Arg223_Leu224delinsMet
ENST00000367030.7:c.668_670del ENSP00000355997.3:p.Arg223_Leu224delinsMet
ENST00000391911.5:c.668_670del ENSP00000375778.1:p.Arg223_Leu224delinsMet
NM_000228.2:c.668_670del NP_000219.2:p.Arg223_Leu224delinsMet
NM_001017402.1:c.668_670del NP_001017402.1:p.Arg223_Leu224delinsMet
NM_001127641.1:c.668_670del NP_001121113.1:p.Arg223_Leu224delinsMet
XM_005273124.3:c.668_670del XP_005273181.1:p.Arg223_Leu224delinsMet
XM_005273124.4:c.668_670del XP_005273181.1:p.Arg223_Leu224delinsMet
XM_017001272.2:c.476_478del XP_016856761.1:p.Arg159_Leu160delinsMet
NM_000228.3:c.668_670del MANE Select NP_000219.2:p.Arg223_Leu224delinsMet
NM_001017402.2:c.668_670del NP_001017402.1:p.Arg223_Leu224delinsMet