Canonical Allele Identifier: CA1732870574

Gene: LAMB1 DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107931411G= , CM000669.2:g.107931411G=	GRCh38
NC_000007.13:g.107571856G= , CM000669.1:g.107571856G=	GRCh37
NC_000007.12:g.107359092G=	NCBI36
NG_023255.1:g.76949C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222399.11:c.4482C= (LAMB1) MANE Select	ENSP00000222399.6:p.Asp1494=
ENST00000393561.6:c.4071C= (LAMB1)	ENSP00000377191.2:p.Asp1357=
ENST00000468518.2:n.2716C= (LAMB1)
ENST00000468999.2:n.2630C= (LAMB1)
ENST00000474380.2:n.1297C= (LAMB1)
ENST00000676574.1:c.*398C= (LAMB1)	ENSP00000503081.1:n.*398C=
ENST00000676744.1:n.328C= (LAMB1)
ENST00000676777.1:c.4482C= (LAMB1)	ENSP00000504756.1:p.Asp1494=
ENST00000677101.1:c.*4118C= (LAMB1)	ENSP00000503156.1:n.*4118C=
ENST00000677144.1:c.*1301C= (LAMB1)	ENSP00000503049.1:n.*1301C=
ENST00000677485.1:n.5706C= (LAMB1)
ENST00000677588.1:c.*713C= (LAMB1)	ENSP00000502938.1:n.*713C=
ENST00000677793.1:c.4170C= (LAMB1)	ENSP00000504020.1:p.Asp1390=
ENST00000677801.1:c.*311C= (LAMB1)	ENSP00000503438.1:n.*311C=
ENST00000678232.1:n.4671C= (LAMB1)
ENST00000678310.1:n.2651C= (LAMB1)
ENST00000678698.1:c.*554C= (LAMB1)	ENSP00000503198.1:n.*554C=
ENST00000678704.1:c.*3064C= (LAMB1)	ENSP00000504589.1:n.*3064C=
ENST00000678892.1:c.*554C= (LAMB1)	ENSP00000504841.1:n.*554C=
ENST00000679200.1:c.*554C= (LAMB1)	ENSP00000503498.1:n.*554C=
ENST00000222399.10:c.4482C= (LAMB1)	ENSP00000222399.6:p.Asp1494=
ENST00000393561.5:c.4554C= (LAMB1)	ENSP00000377191.1:p.Asp1518=
ENST00000417551.5:c.*125-20G= (DLD)	ENSP00000390667.1:n.*125-20G=
ENST00000468518.1:n.541C= (LAMB1)
ENST00000474380.1:n.719C= (LAMB1)
NM_002291.2:c.4482C= (LAMB1)	NP_002282.2:p.Asp1494=
XM_017012201.1:c.4554C= (LAMB1)	XP_016867690.1:p.Asp1518=
XR_001744756.1:n.5401C= (LAMB1)
NM_002291.3:c.4482C= (LAMB1) MANE Select	NP_002282.2:p.Asp1494=