Canonical Allele Identifier: CA2484295758
Gene: LAMB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209617208_209617209delinsTG , CM000663.2:g.209617208_209617209delinsTG GRCh38
NC_000001.10:g.209790553_209790554delinsTG , CM000663.1:g.209790553_209790554delinsTG GRCh37
NC_000001.9:g.207857176_207857177delinsTG NCBI36
NG_007116.1:g.40267_40268delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.3228+201_3228+202delinsCA MANE Select ENSP00000348384.3:n.3228+201_3228+202delinsCA
ENST00000356082.8:c.3228+201_3228+202delinsCA ENSP00000348384.3:n.3228+201_3228+202delinsCA
ENST00000367030.7:c.3228+201_3228+202delinsCA ENSP00000355997.3:n.3228+201_3228+202delinsCA
ENST00000391911.5:c.3228+201_3228+202delinsCA ENSP00000375778.1:n.3228+201_3228+202delinsCA
ENST00000455193.1:c.435+201_435+202delinsCA ENSP00000398683.1:n.435+201_435+202delinsCA
NM_000228.2:c.3228+201_3228+202delinsCA NP_000219.2:n.3228+201_3228+202delinsCA
NM_001017402.1:c.3228+201_3228+202delinsCA NP_001017402.1:n.3228+201_3228+202delinsCA
NM_001127641.1:c.3228+201_3228+202delinsCA NP_001121113.1:n.3228+201_3228+202delinsCA
XM_005273124.3:c.3228+201_3228+202delinsCA XP_005273181.1:n.3228+201_3228+202delinsCA
XM_005273124.4:c.3228+201_3228+202delinsCA XP_005273181.1:n.3228+201_3228+202delinsCA
XM_017001272.2:c.3036+201_3036+202delinsCA XP_016856761.1:n.3036+201_3036+202delinsCA
NM_000228.3:c.3228+201_3228+202delinsCA MANE Select NP_000219.2:n.3228+201_3228+202delinsCA
NM_001017402.2:c.3228+201_3228+202delinsCA NP_001017402.1:n.3228+201_3228+202delinsCA