Canonical Allele Identifier: CA2580061970

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209634470_209634471delinsCC , CM000663.2:g.209634470_209634471delinsCC	GRCh38
NC_000001.10:g.209807815_209807816delinsCC , CM000663.1:g.209807815_209807816delinsCC	GRCh37
NC_000001.9:g.207874438_207874439delinsCC	NCBI36
NG_007116.1:g.23005_23006delinsGG

Transcript Alleles

HGVS	Amino-acid Change
NM_000228.3:c.540_541delinsGG MANE Select	NP_000219.2:p.Asn181Asp
ENST00000356082.9:c.540_541delinsGG MANE Select	ENSP00000348384.3:p.Asn181Asp
NM_000228.2:c.540_541delinsGG	NP_000219.2:p.Asn181Asp
NM_001017402.1:c.540_541delinsGG	NP_001017402.1:p.Asn181Asp
NM_001017402.2:c.540_541delinsGG	NP_001017402.1:p.Asn181Asp
NM_001127641.1:c.540_541delinsGG	NP_001121113.1:p.Asn181Asp
ENST00000356082.8:c.540_541delinsGG	ENSP00000348384.3:p.Asn181Asp
ENST00000367030.7:c.540_541delinsGG	ENSP00000355997.3:p.Asn181Asp
ENST00000391911.5:c.540_541delinsGG	ENSP00000375778.1:p.Asn181Asp
ENST00000415782.1:c.540_541delinsGG	ENSP00000388960.1:p.Asn181Asp
XM_005273124.3:c.540_541delinsGG	XP_005273181.1:p.Asn181Asp
XM_005273124.4:c.540_541delinsGG	XP_005273181.1:p.Asn181Asp
XM_017001272.2:c.373-1338_373-1337delinsGG	XP_016856761.1:n.373-1338_373-1337delinsGG