Canonical Allele Identifier: CA2484298527
Gene: LAMB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209624178_209624179delinsCA , CM000663.2:g.209624178_209624179delinsCA GRCh38
NC_000001.10:g.209797523_209797524delinsCA , CM000663.1:g.209797523_209797524delinsCA GRCh37
NC_000001.9:g.207864146_207864147delinsCA NCBI36
NG_007116.1:g.33297_33298delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.1977-179_1977-178delinsTG MANE Select ENSP00000348384.3:n.1977-179_1977-178delinsTG
ENST00000356082.8:c.1977-179_1977-178delinsTG ENSP00000348384.3:n.1977-179_1977-178delinsTG
ENST00000367030.7:c.1977-179_1977-178delinsTG ENSP00000355997.3:n.1977-179_1977-178delinsTG
ENST00000391911.5:c.1977-179_1977-178delinsTG ENSP00000375778.1:n.1977-179_1977-178delinsTG
NM_000228.2:c.1977-179_1977-178delinsTG NP_000219.2:n.1977-179_1977-178delinsTG
NM_001017402.1:c.1977-179_1977-178delinsTG NP_001017402.1:n.1977-179_1977-178delinsTG
NM_001127641.1:c.1977-179_1977-178delinsTG NP_001121113.1:n.1977-179_1977-178delinsTG
XM_005273124.3:c.1977-179_1977-178delinsTG XP_005273181.1:n.1977-179_1977-178delinsTG
XM_005273124.4:c.1977-179_1977-178delinsTG XP_005273181.1:n.1977-179_1977-178delinsTG
XM_017001272.2:c.1785-179_1785-178delinsTG XP_016856761.1:n.1785-179_1785-178delinsTG
NM_000228.3:c.1977-179_1977-178delinsTG MANE Select NP_000219.2:n.1977-179_1977-178delinsTG
NM_001017402.2:c.1977-179_1977-178delinsTG NP_001017402.1:n.1977-179_1977-178delinsTG