Canonical Allele Identifier: CA1011768218

Gene: LAMB3

Linked Data

• gnomAD v3: 1-209629834-A-ATTGTCACACACACCTCCATATGCCCCATGGCTGGCGGCAAACACAGCGGGGTCAAAGTGACATGTCTCTGAGTGCCC
• gnomAD v4: 1-209629834-A-ATTGTCACACACACCTCCATATGCCCCATGGCTGGCGGCAAACACAGCGGGGTCAAAGTGACATGTCTCTGAGTGCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209629860_209629861insATGGCTGGCGGCAAACACAGCGGGGTCAAAGTGACATGTCTCTGAGTGCCCTTGTCACACACACCTCCATATGCCCC , CM000663.2:g.209629860_209629861insATGGCTGGCGGCAAACACAGCGGGGTCAAAGTGACATGTCTCTGAGTGCCCTTGTCACACACACCTCCATATGCCCC	GRCh38
NC_000001.10:g.209803205_209803206insATGGCTGGCGGCAAACACAGCGGGGTCAAAGTGACATGTCTCTGAGTGCCCTTGTCACACACACCTCCATATGCCCC , CM000663.1:g.209803205_209803206insATGGCTGGCGGCAAACACAGCGGGGTCAAAGTGACATGTCTCTGAGTGCCCTTGTCACACACACCTCCATATGCCCC	GRCh37
NC_000001.9:g.207869828_207869829insATGGCTGGCGGCAAACACAGCGGGGTCAAAGTGACATGTCTCTGAGTGCCCTTGTCACACACACCTCCATATGCCCC	NCBI36
NG_007116.1:g.27641_27642insGGGCACTCAGAGACATGTCACTTTGACCCCGCTGTGTTTGCCGCCAGCCATGGGGCATATGGAGGTGTGTGTGACAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.1034_1035insGGGCACTCAGAGACATGTCACTTTGACCCCGCTGTGTTTGCCGCCAGCCATGGGGCATATGGAGGTGTGTGTGACAA MANE Select	ENSP00000348384.3:p.Asn345LysfsTer?
ENST00000356082.8:c.1034_1035insGGGCACTCAGAGACATGTCACTTTGACCCCGCTGTGTTTGCCGCCAGCCATGGGGCATATGGAGGTGTGTGTGACAA	ENSP00000348384.3:p.Asn345LysfsTer?
ENST00000367030.7:c.1034_1035insGGGCACTCAGAGACATGTCACTTTGACCCCGCTGTGTTTGCCGCCAGCCATGGGGCATATGGAGGTGTGTGTGACAA	ENSP00000355997.3:p.Asn345LysfsTer?
ENST00000391911.5:c.1034_1035insGGGCACTCAGAGACATGTCACTTTGACCCCGCTGTGTTTGCCGCCAGCCATGGGGCATATGGAGGTGTGTGTGACAA	ENSP00000375778.1:p.Asn345LysfsTer?
NM_000228.2:c.1034_1035insGGGCACTCAGAGACATGTCACTTTGACCCCGCTGTGTTTGCCGCCAGCCATGGGGCATATGGAGGTGTGTGTGACAA	NP_000219.2:p.Asn345LysfsTer?
NM_001017402.1:c.1034_1035insGGGCACTCAGAGACATGTCACTTTGACCCCGCTGTGTTTGCCGCCAGCCATGGGGCATATGGAGGTGTGTGTGACAA	NP_001017402.1:p.Asn345LysfsTer?
NM_001127641.1:c.1034_1035insGGGCACTCAGAGACATGTCACTTTGACCCCGCTGTGTTTGCCGCCAGCCATGGGGCATATGGAGGTGTGTGTGACAA	NP_001121113.1:p.Asn345LysfsTer?
XM_005273124.3:c.1034_1035insGGGCACTCAGAGACATGTCACTTTGACCCCGCTGTGTTTGCCGCCAGCCATGGGGCATATGGAGGTGTGTGTGACAA	XP_005273181.1:p.Asn345LysfsTer?
XM_005273124.4:c.1034_1035insGGGCACTCAGAGACATGTCACTTTGACCCCGCTGTGTTTGCCGCCAGCCATGGGGCATATGGAGGTGTGTGTGACAA	XP_005273181.1:p.Asn345LysfsTer?
XM_017001272.2:c.842_843insGGGCACTCAGAGACATGTCACTTTGACCCCGCTGTGTTTGCCGCCAGCCATGGGGCATATGGAGGTGTGTGTGACAA	XP_016856761.1:p.Asn281LysfsTer?
NM_000228.3:c.1034_1035insGGGCACTCAGAGACATGTCACTTTGACCCCGCTGTGTTTGCCGCCAGCCATGGGGCATATGGAGGTGTGTGTGACAA MANE Select	NP_000219.2:p.Asn345LysfsTer?
NM_001017402.2:c.1034_1035insGGGCACTCAGAGACATGTCACTTTGACCCCGCTGTGTTTGCCGCCAGCCATGGGGCATATGGAGGTGTGTGTGACAA	NP_001017402.1:p.Asn345LysfsTer?