Canonical Allele Identifier: CA2756174308

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49122880_49122881insGT , CM000665.2:g.49122880_49122881insGT	GRCh38
NC_000003.11:g.49160313_49160314insGT , CM000665.1:g.49160313_49160314insGT	GRCh37
NC_000003.10:g.49135317_49135318insGT	NCBI36
NG_008094.1:g.15286_15287insAC
NG_054716.1:g.3058_3059insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.4396_4397insAC MANE Select	ENSP00000307156.4:p.Ala1466AspfsTer?
ENST00000305544.8:c.4396_4397insAC	ENSP00000307156.4:p.Ala1466AspfsTer?
ENST00000418109.5:c.4396_4397insAC	ENSP00000388325.1:p.Ala1466AspfsTer?
ENST00000469665.1:n.705_706insAC
NM_002292.3:c.4396_4397insAC	NP_002283.3:p.Ala1466AspfsTer?
XM_005265127.3:c.4396_4397insAC	XP_005265184.1:p.Ala1466AspfsTer?
XM_005265127.4:c.4396_4397insAC	XP_005265184.1:p.Ala1466AspfsTer?
NM_002292.4:c.4396_4397insAC MANE Select	NP_002283.3:p.Ala1466AspfsTer?