Canonical Allele Identifier: CA2484295755
Gene: LAMB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209617205_209617206delinsCA , CM000663.2:g.209617205_209617206delinsCA GRCh38
NC_000001.10:g.209790550_209790551delinsCA , CM000663.1:g.209790550_209790551delinsCA GRCh37
NC_000001.9:g.207857173_207857174delinsCA NCBI36
NG_007116.1:g.40270_40271delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.3228+204_3228+205delinsTG MANE Select ENSP00000348384.3:n.3228+204_3228+205delinsTG
ENST00000356082.8:c.3228+204_3228+205delinsTG ENSP00000348384.3:n.3228+204_3228+205delinsTG
ENST00000367030.7:c.3228+204_3228+205delinsTG ENSP00000355997.3:n.3228+204_3228+205delinsTG
ENST00000391911.5:c.3228+204_3228+205delinsTG ENSP00000375778.1:n.3228+204_3228+205delinsTG
ENST00000455193.1:c.435+204_435+205delinsTG ENSP00000398683.1:n.435+204_435+205delinsTG
NM_000228.2:c.3228+204_3228+205delinsTG NP_000219.2:n.3228+204_3228+205delinsTG
NM_001017402.1:c.3228+204_3228+205delinsTG NP_001017402.1:n.3228+204_3228+205delinsTG
NM_001127641.1:c.3228+204_3228+205delinsTG NP_001121113.1:n.3228+204_3228+205delinsTG
XM_005273124.3:c.3228+204_3228+205delinsTG XP_005273181.1:n.3228+204_3228+205delinsTG
XM_005273124.4:c.3228+204_3228+205delinsTG XP_005273181.1:n.3228+204_3228+205delinsTG
XM_017001272.2:c.3036+204_3036+205delinsTG XP_016856761.1:n.3036+204_3036+205delinsTG
NM_000228.3:c.3228+204_3228+205delinsTG MANE Select NP_000219.2:n.3228+204_3228+205delinsTG
NM_001017402.2:c.3228+204_3228+205delinsTG NP_001017402.1:n.3228+204_3228+205delinsTG