Canonical Allele Identifier: CA2607036471
Gene: LAMB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209618418_209618421del , CM000663.2:g.209618418_209618421del GRCh38
NC_000001.10:g.209791763_209791766del , CM000663.1:g.209791763_209791766del GRCh37
NC_000001.9:g.207858386_207858389del NCBI36
NG_007116.1:g.39055_39058del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.2909+31_2909+34del MANE Select ENSP00000348384.3:n.2909+31_2909+34del
ENST00000356082.8:c.2909+31_2909+34del ENSP00000348384.3:n.2909+31_2909+34del
ENST00000367030.7:c.2909+31_2909+34del ENSP00000355997.3:n.2909+31_2909+34del
ENST00000391911.5:c.2909+31_2909+34del ENSP00000375778.1:n.2909+31_2909+34del
ENST00000455193.1:c.116+31_116+34del ENSP00000398683.1:n.116+31_116+34del
NM_000228.2:c.2909+31_2909+34del NP_000219.2:n.2909+31_2909+34del
NM_001017402.1:c.2909+31_2909+34del NP_001017402.1:n.2909+31_2909+34del
NM_001127641.1:c.2909+31_2909+34del NP_001121113.1:n.2909+31_2909+34del
XM_005273124.3:c.2909+31_2909+34del XP_005273181.1:n.2909+31_2909+34del
XM_005273124.4:c.2909+31_2909+34del XP_005273181.1:n.2909+31_2909+34del
XM_017001272.2:c.2717+31_2717+34del XP_016856761.1:n.2717+31_2717+34del
NM_000228.3:c.2909+31_2909+34del MANE Select NP_000219.2:n.2909+31_2909+34del
NM_001017402.2:c.2909+31_2909+34del NP_001017402.1:n.2909+31_2909+34del