Canonical Allele Identifier: CA2697554864
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2704245
ClinVar RCV Id: RCV003572850

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209618539del , CM000663.2:g.209618539del GRCh38
NC_000001.10:g.209791884del , CM000663.1:g.209791884del GRCh37
NC_000001.9:g.207858507del NCBI36
NG_007116.1:g.38938del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.2823del MANE Select ENSP00000348384.3:p.Arg941SerfsTer?
ENST00000356082.8:c.2823del ENSP00000348384.3:p.Arg941SerfsTer?
ENST00000367030.7:c.2823del ENSP00000355997.3:p.Arg941SerfsTer?
ENST00000391911.5:c.2823del ENSP00000375778.1:p.Arg941SerfsTer?
ENST00000455193.1:c.30del ENSP00000398683.1:p.Arg10SerfsTer?
NM_000228.2:c.2823del NP_000219.2:p.Arg941SerfsTer?
NM_001017402.1:c.2823del NP_001017402.1:p.Arg941SerfsTer?
NM_001127641.1:c.2823del NP_001121113.1:p.Arg941SerfsTer?
XM_005273124.3:c.2823del XP_005273181.1:p.Arg941SerfsTer?
XM_005273124.4:c.2823del XP_005273181.1:p.Arg941SerfsTer?
XM_017001272.2:c.2631del XP_016856761.1:p.Arg877SerfsTer?
NM_000228.3:c.2823del MANE Select NP_000219.2:p.Arg941SerfsTer?
NM_001017402.2:c.2823del NP_001017402.1:p.Arg941SerfsTer?