Canonical Allele Identifier: CA2484296275

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209618499_209618500delinsCT , CM000663.2:g.209618499_209618500delinsCT	GRCh38
NC_000001.10:g.209791844_209791845delinsCT , CM000663.1:g.209791844_209791845delinsCT	GRCh37
NC_000001.9:g.207858467_207858468delinsCT	NCBI36
NG_007116.1:g.38976_38977delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.2861_2862delinsAG MANE Select	ENSP00000348384.3:p.Gln954=
ENST00000356082.8:c.2861_2862delinsAG	ENSP00000348384.3:p.Gln954=
ENST00000367030.7:c.2861_2862delinsAG	ENSP00000355997.3:p.Gln954=
ENST00000391911.5:c.2861_2862delinsAG	ENSP00000375778.1:p.Gln954=
ENST00000455193.1:c.68_69delinsAG	ENSP00000398683.1:p.Gln23=
NM_000228.2:c.2861_2862delinsAG	NP_000219.2:p.Gln954=
NM_001017402.1:c.2861_2862delinsAG	NP_001017402.1:p.Gln954=
NM_001127641.1:c.2861_2862delinsAG	NP_001121113.1:p.Gln954=
XM_005273124.3:c.2861_2862delinsAG	XP_005273181.1:p.Gln954=
XM_005273124.4:c.2861_2862delinsAG	XP_005273181.1:p.Gln954=
XM_017001272.2:c.2669_2670delinsAG	XP_016856761.1:p.Gln890=
NM_000228.3:c.2861_2862delinsAG MANE Select	NP_000219.2:p.Gln954=
NM_001017402.2:c.2861_2862delinsAG	NP_001017402.1:p.Gln954=