Canonical Allele Identifier: CA1149041319

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209617936_209617938delinsGGG , CM000663.2:g.209617936_209617938delinsGGG	GRCh38
NC_000001.10:g.209791281_209791283delinsGGG , CM000663.1:g.209791281_209791283delinsGGG	GRCh37
NC_000001.9:g.207857904_207857906delinsGGG	NCBI36
NG_007116.1:g.39538_39540delinsCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.3020_3022delinsCCC MANE Select	ENSP00000348384.3:p.Ser1007=
ENST00000356082.8:c.3020_3022delinsCCC	ENSP00000348384.3:p.Ser1007=
ENST00000367030.7:c.3020_3022delinsCCC	ENSP00000355997.3:p.Ser1007=
ENST00000391911.5:c.3020_3022delinsCCC	ENSP00000375778.1:p.Ser1007=
ENST00000455193.1:c.227_229delinsCCC	ENSP00000398683.1:p.Ser76=
NM_000228.2:c.3020_3022delinsCCC	NP_000219.2:p.Ser1007=
NM_001017402.1:c.3020_3022delinsCCC	NP_001017402.1:p.Ser1007=
NM_001127641.1:c.3020_3022delinsCCC	NP_001121113.1:p.Ser1007=
XM_005273124.3:c.3020_3022delinsCCC	XP_005273181.1:p.Ser1007=
XM_005273124.4:c.3020_3022delinsCCC	XP_005273181.1:p.Ser1007=
XM_017001272.2:c.2828_2830delinsCCC	XP_016856761.1:p.Ser943=
NM_000228.3:c.3020_3022delinsCCC MANE Select	NP_000219.2:p.Ser1007=
NM_001017402.2:c.3020_3022delinsCCC	NP_001017402.1:p.Ser1007=