Canonical Allele Identifier: CA2484309187
Gene: LAMB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209649654_209649655delinsTG , CM000663.2:g.209649654_209649655delinsTG GRCh38
NC_000001.10:g.209822999_209823000delinsTG , CM000663.1:g.209822999_209823000delinsTG GRCh37
NC_000001.9:g.207889622_207889623delinsTG NCBI36
NG_007116.1:g.7821_7822delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.183+309_183+310delinsCA MANE Select ENSP00000348384.3:n.183+309_183+310delinsCA
ENST00000356082.8:c.183+309_183+310delinsCA ENSP00000348384.3:n.183+309_183+310delinsCA
ENST00000367030.7:c.183+309_183+310delinsCA ENSP00000355997.3:n.183+309_183+310delinsCA
ENST00000391911.5:c.183+309_183+310delinsCA ENSP00000375778.1:n.183+309_183+310delinsCA
ENST00000415782.1:c.183+309_183+310delinsCA ENSP00000388960.1:n.183+309_183+310delinsCA
NM_000228.2:c.183+309_183+310delinsCA NP_000219.2:n.183+309_183+310delinsCA
NM_001017402.1:c.183+309_183+310delinsCA NP_001017402.1:n.183+309_183+310delinsCA
NM_001127641.1:c.183+309_183+310delinsCA NP_001121113.1:n.183+309_183+310delinsCA
XM_005273124.3:c.183+309_183+310delinsCA XP_005273181.1:n.183+309_183+310delinsCA
XM_005273124.4:c.183+309_183+310delinsCA XP_005273181.1:n.183+309_183+310delinsCA
XM_017001272.2:c.183+309_183+310delinsCA XP_016856761.1:n.183+309_183+310delinsCA
NM_000228.3:c.183+309_183+310delinsCA MANE Select NP_000219.2:n.183+309_183+310delinsCA
NM_001017402.2:c.183+309_183+310delinsCA NP_001017402.1:n.183+309_183+310delinsCA