Canonical Allele Identifier: CA2484296272

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209618494_209618495delinsAT , CM000663.2:g.209618494_209618495delinsAT	GRCh38
NC_000001.10:g.209791839_209791840delinsAT , CM000663.1:g.209791839_209791840delinsAT	GRCh37
NC_000001.9:g.207858462_207858463delinsAT	NCBI36
NG_007116.1:g.38981_38982delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.2866_2867delinsAT MANE Select	ENSP00000348384.3:p.Ile956=
ENST00000356082.8:c.2866_2867delinsAT	ENSP00000348384.3:p.Ile956=
ENST00000367030.7:c.2866_2867delinsAT	ENSP00000355997.3:p.Ile956=
ENST00000391911.5:c.2866_2867delinsAT	ENSP00000375778.1:p.Ile956=
ENST00000455193.1:c.73_74delinsAT	ENSP00000398683.1:p.Ile25=
NM_000228.2:c.2866_2867delinsAT	NP_000219.2:p.Ile956=
NM_001017402.1:c.2866_2867delinsAT	NP_001017402.1:p.Ile956=
NM_001127641.1:c.2866_2867delinsAT	NP_001121113.1:p.Ile956=
XM_005273124.3:c.2866_2867delinsAT	XP_005273181.1:p.Ile956=
XM_005273124.4:c.2866_2867delinsAT	XP_005273181.1:p.Ile956=
XM_017001272.2:c.2674_2675delinsAT	XP_016856761.1:p.Ile892=
NM_000228.3:c.2866_2867delinsAT MANE Select	NP_000219.2:p.Ile956=
NM_001017402.2:c.2866_2867delinsAT	NP_001017402.1:p.Ile956=