Canonical Allele Identifier: CA2484296035
Gene: LAMB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209617880_209617881delinsTG , CM000663.2:g.209617880_209617881delinsTG GRCh38
NC_000001.10:g.209791225_209791226delinsTG , CM000663.1:g.209791225_209791226delinsTG GRCh37
NC_000001.9:g.207857848_207857849delinsTG NCBI36
NG_007116.1:g.39595_39596delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.3051+26_3051+27delinsCA MANE Select ENSP00000348384.3:n.3051+26_3051+27delinsCA
ENST00000356082.8:c.3051+26_3051+27delinsCA ENSP00000348384.3:n.3051+26_3051+27delinsCA
ENST00000367030.7:c.3051+26_3051+27delinsCA ENSP00000355997.3:n.3051+26_3051+27delinsCA
ENST00000391911.5:c.3051+26_3051+27delinsCA ENSP00000375778.1:n.3051+26_3051+27delinsCA
ENST00000455193.1:c.258+26_258+27delinsCA ENSP00000398683.1:n.258+26_258+27delinsCA
NM_000228.2:c.3051+26_3051+27delinsCA NP_000219.2:n.3051+26_3051+27delinsCA
NM_001017402.1:c.3051+26_3051+27delinsCA NP_001017402.1:n.3051+26_3051+27delinsCA
NM_001127641.1:c.3051+26_3051+27delinsCA NP_001121113.1:n.3051+26_3051+27delinsCA
XM_005273124.3:c.3051+26_3051+27delinsCA XP_005273181.1:n.3051+26_3051+27delinsCA
XM_005273124.4:c.3051+26_3051+27delinsCA XP_005273181.1:n.3051+26_3051+27delinsCA
XM_017001272.2:c.2859+26_2859+27delinsCA XP_016856761.1:n.2859+26_2859+27delinsCA
NM_000228.3:c.3051+26_3051+27delinsCA MANE Select NP_000219.2:n.3051+26_3051+27delinsCA
NM_001017402.2:c.3051+26_3051+27delinsCA NP_001017402.1:n.3051+26_3051+27delinsCA