Canonical Allele Identifier: CA2840215335

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209615350del , CM000663.2:g.209615350del	GRCh38
NC_000001.10:g.209788695del , CM000663.1:g.209788695del	GRCh37
NC_000001.9:g.207855318del	NCBI36
NG_007116.1:g.42126del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.3440del MANE Select	ENSP00000348384.3:p.Leu1147ArgfsTer?
ENST00000356082.8:c.3440del	ENSP00000348384.3:p.Leu1147ArgfsTer?
ENST00000367030.7:c.3440del	ENSP00000355997.3:p.Leu1147ArgfsTer?
ENST00000391911.5:c.3440del	ENSP00000375778.1:p.Leu1147ArgfsTer?
NM_000228.2:c.3440del	NP_000219.2:p.Leu1147ArgfsTer?
NM_001017402.1:c.3440del	NP_001017402.1:p.Leu1147ArgfsTer?
NM_001127641.1:c.3440del	NP_001121113.1:p.Leu1147ArgfsTer?
XM_005273124.3:c.3440del	XP_005273181.1:p.Leu1147ArgfsTer?
XM_005273124.4:c.3440del	XP_005273181.1:p.Leu1147ArgfsTer?
XM_017001272.2:c.3248del	XP_016856761.1:p.Leu1083ArgfsTer?
NM_000228.3:c.3440del MANE Select	NP_000219.2:p.Leu1147ArgfsTer?
NM_001017402.2:c.3440del	NP_001017402.1:p.Leu1147ArgfsTer?