Canonical Allele Identifier: CA2484296059

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209617935_209617936delinsAG , CM000663.2:g.209617935_209617936delinsAG	GRCh38
NC_000001.10:g.209791280_209791281delinsAG , CM000663.1:g.209791280_209791281delinsAG	GRCh37
NC_000001.9:g.207857903_207857904delinsAG	NCBI36
NG_007116.1:g.39540_39541delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.3022_3023delinsCT MANE Select	ENSP00000348384.3:p.Leu1008=
ENST00000356082.8:c.3022_3023delinsCT	ENSP00000348384.3:p.Leu1008=
ENST00000367030.7:c.3022_3023delinsCT	ENSP00000355997.3:p.Leu1008=
ENST00000391911.5:c.3022_3023delinsCT	ENSP00000375778.1:p.Leu1008=
ENST00000455193.1:c.229_230delinsCT	ENSP00000398683.1:p.Leu77=
NM_000228.2:c.3022_3023delinsCT	NP_000219.2:p.Leu1008=
NM_001017402.1:c.3022_3023delinsCT	NP_001017402.1:p.Leu1008=
NM_001127641.1:c.3022_3023delinsCT	NP_001121113.1:p.Leu1008=
XM_005273124.3:c.3022_3023delinsCT	XP_005273181.1:p.Leu1008=
XM_005273124.4:c.3022_3023delinsCT	XP_005273181.1:p.Leu1008=
XM_017001272.2:c.2830_2831delinsCT	XP_016856761.1:p.Leu944=
NM_000228.3:c.3022_3023delinsCT MANE Select	NP_000219.2:p.Leu1008=
NM_001017402.2:c.3022_3023delinsCT	NP_001017402.1:p.Leu1008=