Canonical Allele Identifier: CA2573998399
Gene: LAMB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209624033del , CM000663.2:g.209624033del GRCh38
NC_000001.10:g.209797378del , CM000663.1:g.209797378del GRCh37
NC_000001.9:g.207864001del NCBI36
NG_007116.1:g.33443del

Transcript Alleles

HGVS Amino-acid change
ENST00000356082.9:c.1977-33del MANE Select ENSP00000348384.3:n.1977-33del
ENST00000356082.8:c.1977-33del ENSP00000348384.3:n.1977-33del
ENST00000367030.7:c.1977-33del ENSP00000355997.3:n.1977-33del
ENST00000391911.5:c.1977-33del ENSP00000375778.1:n.1977-33del
NM_000228.2:c.1977-33del NP_000219.2:n.1977-33del
NM_001017402.1:c.1977-33del NP_001017402.1:n.1977-33del
NM_001127641.1:c.1977-33del NP_001121113.1:n.1977-33del
XM_005273124.3:c.1977-33del XP_005273181.1:n.1977-33del
XM_005273124.4:c.1977-33del XP_005273181.1:n.1977-33del
XM_017001272.2:c.1785-33del XP_016856761.1:n.1785-33del
NM_000228.3:c.1977-33del MANE Select NP_000219.2:n.1977-33del
NM_001017402.2:c.1977-33del NP_001017402.1:n.1977-33del