Canonical Allele Identifier: CA1144103623
Gene: LAMB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209633321_209633334delinsGTGTGTGTGTGTGT , CM000663.2:g.209633321_209633334delinsGTGTGTGTGTGTGT GRCh38
NC_000001.10:g.209806666_209806679delinsGTGTGTGTGTGTGT , CM000663.1:g.209806666_209806679delinsGTGTGTGTGTGTGT GRCh37
NC_000001.9:g.207873289_207873302delinsGTGTGTGTGTGTGT NCBI36
NG_007116.1:g.24142_24155delinsACACACACACACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.565-201_565-188delinsACACACACACACAC MANE Select ENSP00000348384.3:n.565-201_565-188delinsACACACACACACAC
ENST00000356082.8:c.565-201_565-188delinsACACACACACACAC ENSP00000348384.3:n.565-201_565-188delinsACACACACACACAC
ENST00000367030.7:c.565-201_565-188delinsACACACACACACAC ENSP00000355997.3:n.565-201_565-188delinsACACACACACACAC
ENST00000391911.5:c.565-201_565-188delinsACACACACACACAC ENSP00000375778.1:n.565-201_565-188delinsACACACACACACAC
NM_000228.2:c.565-201_565-188delinsACACACACACACAC NP_000219.2:n.565-201_565-188delinsACACACACACACAC
NM_001017402.1:c.565-201_565-188delinsACACACACACACAC NP_001017402.1:n.565-201_565-188delinsACACACACACACAC
NM_001127641.1:c.565-201_565-188delinsACACACACACACAC NP_001121113.1:n.565-201_565-188delinsACACACACACACAC
XM_005273124.3:c.565-201_565-188delinsACACACACACACAC XP_005273181.1:n.565-201_565-188delinsACACACACACACAC
XM_005273124.4:c.565-201_565-188delinsACACACACACACAC XP_005273181.1:n.565-201_565-188delinsACACACACACACAC
XM_017001272.2:c.373-201_373-188delinsACACACACACACAC XP_016856761.1:n.373-201_373-188delinsACACACACACACAC
NM_000228.3:c.565-201_565-188delinsACACACACACACAC MANE Select NP_000219.2:n.565-201_565-188delinsACACACACACACAC
NM_001017402.2:c.565-201_565-188delinsACACACACACACAC NP_001017402.1:n.565-201_565-188delinsACACACACACACAC