Canonical Allele Identifier: CA2484300833

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209629802_209629804delinsTCA , CM000663.2:g.209629802_209629804delinsTCA	GRCh38
NC_000001.10:g.209803147_209803149delinsTCA , CM000663.1:g.209803147_209803149delinsTCA	GRCh37
NC_000001.9:g.207869770_207869772delinsTCA	NCBI36
NG_007116.1:g.27672_27674delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.1065_1067delinsTGA MANE Select	ENSP00000348384.3:p.Cys355=
ENST00000356082.8:c.1065_1067delinsTGA	ENSP00000348384.3:p.Cys355=
ENST00000367030.7:c.1065_1067delinsTGA	ENSP00000355997.3:p.Cys355=
ENST00000391911.5:c.1065_1067delinsTGA	ENSP00000375778.1:p.Cys355=
NM_000228.2:c.1065_1067delinsTGA	NP_000219.2:p.Cys355=
NM_001017402.1:c.1065_1067delinsTGA	NP_001017402.1:p.Cys355=
NM_001127641.1:c.1065_1067delinsTGA	NP_001121113.1:p.Cys355=
XM_005273124.3:c.1065_1067delinsTGA	XP_005273181.1:p.Cys355=
XM_005273124.4:c.1065_1067delinsTGA	XP_005273181.1:p.Cys355=
XM_017001272.2:c.873_875delinsTGA	XP_016856761.1:p.Cys291=
NM_000228.3:c.1065_1067delinsTGA MANE Select	NP_000219.2:p.Cys355=
NM_001017402.2:c.1065_1067delinsTGA	NP_001017402.1:p.Cys355=