Canonical Allele Identifier: CA2573998463
Gene: LAMB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209624081_209624086del , CM000663.2:g.209624081_209624086del GRCh38
NC_000001.10:g.209797426_209797431del , CM000663.1:g.209797426_209797431del GRCh37
NC_000001.9:g.207864049_207864054del NCBI36
NG_007116.1:g.33394_33399del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.1977-82_1977-77del MANE Select ENSP00000348384.3:n.1977-82_1977-77del
ENST00000356082.8:c.1977-82_1977-77del ENSP00000348384.3:n.1977-82_1977-77del
ENST00000367030.7:c.1977-82_1977-77del ENSP00000355997.3:n.1977-82_1977-77del
ENST00000391911.5:c.1977-82_1977-77del ENSP00000375778.1:n.1977-82_1977-77del
NM_000228.2:c.1977-82_1977-77del NP_000219.2:n.1977-82_1977-77del
NM_001017402.1:c.1977-82_1977-77del NP_001017402.1:n.1977-82_1977-77del
NM_001127641.1:c.1977-82_1977-77del NP_001121113.1:n.1977-82_1977-77del
XM_005273124.3:c.1977-82_1977-77del XP_005273181.1:n.1977-82_1977-77del
XM_005273124.4:c.1977-82_1977-77del XP_005273181.1:n.1977-82_1977-77del
XM_017001272.2:c.1785-82_1785-77del XP_016856761.1:n.1785-82_1785-77del
NM_000228.3:c.1977-82_1977-77del MANE Select NP_000219.2:n.1977-82_1977-77del
NM_001017402.2:c.1977-82_1977-77del NP_001017402.1:n.1977-82_1977-77del