Canonical Allele Identifier: CA2650320597
Gene: LAMB3 HGNC NCBI

Linked Data

gnomAD v4: 1-209618377-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209618380del , CM000663.2:g.209618380del GRCh38
NC_000001.10:g.209791725del , CM000663.1:g.209791725del GRCh37
NC_000001.9:g.207858348del NCBI36
NG_007116.1:g.39098del

Transcript Alleles

HGVS Amino-acid change
ENST00000356082.9:c.2909+74del MANE Select ENSP00000348384.3:n.2909+74del
ENST00000356082.8:c.2909+74del ENSP00000348384.3:n.2909+74del
ENST00000367030.7:c.2909+74del ENSP00000355997.3:n.2909+74del
ENST00000391911.5:c.2909+74del ENSP00000375778.1:n.2909+74del
ENST00000455193.1:c.116+74del ENSP00000398683.1:n.116+74del
NM_000228.2:c.2909+74del NP_000219.2:n.2909+74del
NM_001017402.1:c.2909+74del NP_001017402.1:n.2909+74del
NM_001127641.1:c.2909+74del NP_001121113.1:n.2909+74del
XM_005273124.3:c.2909+74del XP_005273181.1:n.2909+74del
XM_005273124.4:c.2909+74del XP_005273181.1:n.2909+74del
XM_017001272.2:c.2717+74del XP_016856761.1:n.2717+74del
NM_000228.3:c.2909+74del MANE Select NP_000219.2:n.2909+74del
NM_001017402.2:c.2909+74del NP_001017402.1:n.2909+74del
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