Canonical Allele Identifier: CA2484296064
Gene: LAMB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209617941_209617942delinsCG , CM000663.2:g.209617941_209617942delinsCG GRCh38
NC_000001.10:g.209791286_209791287delinsCG , CM000663.1:g.209791286_209791287delinsCG GRCh37
NC_000001.9:g.207857909_207857910delinsCG NCBI36
NG_007116.1:g.39534_39535delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.3016_3017delinsCG MANE Select ENSP00000348384.3:p.Arg1006=
ENST00000356082.8:c.3016_3017delinsCG ENSP00000348384.3:p.Arg1006=
ENST00000367030.7:c.3016_3017delinsCG ENSP00000355997.3:p.Arg1006=
ENST00000391911.5:c.3016_3017delinsCG ENSP00000375778.1:p.Arg1006=
ENST00000455193.1:c.223_224delinsCG ENSP00000398683.1:p.Arg75=
NM_000228.2:c.3016_3017delinsCG NP_000219.2:p.Arg1006=
NM_001017402.1:c.3016_3017delinsCG NP_001017402.1:p.Arg1006=
NM_001127641.1:c.3016_3017delinsCG NP_001121113.1:p.Arg1006=
XM_005273124.3:c.3016_3017delinsCG XP_005273181.1:p.Arg1006=
XM_005273124.4:c.3016_3017delinsCG XP_005273181.1:p.Arg1006=
XM_017001272.2:c.2824_2825delinsCG XP_016856761.1:p.Arg942=
NM_000228.3:c.3016_3017delinsCG MANE Select NP_000219.2:p.Arg1006=
NM_001017402.2:c.3016_3017delinsCG NP_001017402.1:p.Arg1006=