Canonical Allele Identifier: CA2650324117
Gene: LAMB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209650205del , CM000663.2:g.209650205del GRCh38
NC_000001.10:g.209823550del , CM000663.1:g.209823550del GRCh37
NC_000001.9:g.207890173del NCBI36
NG_007116.1:g.7272del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.29-86del MANE Select ENSP00000348384.3:n.29-86del
ENST00000356082.8:c.29-86del ENSP00000348384.3:n.29-86del
ENST00000367030.7:c.29-86del ENSP00000355997.3:n.29-86del
ENST00000391911.5:c.29-86del ENSP00000375778.1:n.29-86del
ENST00000415782.1:c.29-86del ENSP00000388960.1:n.29-86del
NM_000228.2:c.29-86del NP_000219.2:n.29-86del
NM_001017402.1:c.29-86del NP_001017402.1:n.29-86del
NM_001127641.1:c.29-86del NP_001121113.1:n.29-86del
XM_005273124.3:c.29-86del XP_005273181.1:n.29-86del
XM_005273124.4:c.29-86del XP_005273181.1:n.29-86del
XM_017001272.2:c.29-86del XP_016856761.1:n.29-86del
NM_000228.3:c.29-86del MANE Select NP_000219.2:n.29-86del
NM_001017402.2:c.29-86del NP_001017402.1:n.29-86del