Canonical Allele Identifier: CA2484300856

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209629861_209629862delinsCT , CM000663.2:g.209629861_209629862delinsCT	GRCh38
NC_000001.10:g.209803206_209803207delinsCT , CM000663.1:g.209803206_209803207delinsCT	GRCh37
NC_000001.9:g.207869829_207869830delinsCT	NCBI36
NG_007116.1:g.27614_27615delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.1007_1008delinsAG MANE Select	ENSP00000348384.3:p.Gln336=
ENST00000356082.8:c.1007_1008delinsAG	ENSP00000348384.3:p.Gln336=
ENST00000367030.7:c.1007_1008delinsAG	ENSP00000355997.3:p.Gln336=
ENST00000391911.5:c.1007_1008delinsAG	ENSP00000375778.1:p.Gln336=
NM_000228.2:c.1007_1008delinsAG	NP_000219.2:p.Gln336=
NM_001017402.1:c.1007_1008delinsAG	NP_001017402.1:p.Gln336=
NM_001127641.1:c.1007_1008delinsAG	NP_001121113.1:p.Gln336=
XM_005273124.3:c.1007_1008delinsAG	XP_005273181.1:p.Gln336=
XM_005273124.4:c.1007_1008delinsAG	XP_005273181.1:p.Gln336=
XM_017001272.2:c.815_816delinsAG	XP_016856761.1:p.Gln272=
NM_000228.3:c.1007_1008delinsAG MANE Select	NP_000219.2:p.Gln336=
NM_001017402.2:c.1007_1008delinsAG	NP_001017402.1:p.Gln336=