Canonical Allele Identifier: CA2484304440
Gene: LAMB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209638503_209638504delinsGT , CM000663.2:g.209638503_209638504delinsGT GRCh38
NC_000001.10:g.209811848_209811849delinsGT , CM000663.1:g.209811848_209811849delinsGT GRCh37
NC_000001.9:g.207878471_207878472delinsGT NCBI36
NG_007116.1:g.18972_18973delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000356082.9:c.298+30_298+31delinsAC MANE Select ENSP00000348384.3:n.298+30_298+31delinsAC
ENST00000356082.8:c.298+30_298+31delinsAC ENSP00000348384.3:n.298+30_298+31delinsAC
ENST00000367030.7:c.298+30_298+31delinsAC ENSP00000355997.3:n.298+30_298+31delinsAC
ENST00000391911.5:c.298+30_298+31delinsAC ENSP00000375778.1:n.298+30_298+31delinsAC
ENST00000415782.1:c.298+30_298+31delinsAC ENSP00000388960.1:n.298+30_298+31delinsAC
NM_000228.2:c.298+30_298+31delinsAC NP_000219.2:n.298+30_298+31delinsAC
NM_001017402.1:c.298+30_298+31delinsAC NP_001017402.1:n.298+30_298+31delinsAC
NM_001127641.1:c.298+30_298+31delinsAC NP_001121113.1:n.298+30_298+31delinsAC
XM_005273124.3:c.298+30_298+31delinsAC XP_005273181.1:n.298+30_298+31delinsAC
XM_005273124.4:c.298+30_298+31delinsAC XP_005273181.1:n.298+30_298+31delinsAC
XM_017001272.2:c.298+30_298+31delinsAC XP_016856761.1:n.298+30_298+31delinsAC
NM_000228.3:c.298+30_298+31delinsAC MANE Select NP_000219.2:n.298+30_298+31delinsAC
NM_001017402.2:c.298+30_298+31delinsAC NP_001017402.1:n.298+30_298+31delinsAC