Canonical Allele Identifier: CA368864232

Gene: LAMB1 DLD

Linked Data

• MyVariant Identifiers: chr7:g.107571917T>G (hg19) ; chr7:g.107931472T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107931472T>G , CM000669.2:g.107931472T>G	GRCh38
NC_000007.13:g.107571917T>G , CM000669.1:g.107571917T>G	GRCh37
NC_000007.12:g.107359153T>G	NCBI36
NG_023255.1:g.76888A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222399.11:c.4421A>C (LAMB1) MANE Select	ENSP00000222399.6:p.Glu1474Ala
ENST00000393561.6:c.4010A>C (LAMB1)	ENSP00000377191.2:p.Glu1337Ala
ENST00000468518.2:n.2655A>C (LAMB1)
ENST00000468999.2:n.2569A>C (LAMB1)
ENST00000474380.2:n.1236A>C (LAMB1)
ENST00000676574.1:c.*337A>C (LAMB1)	ENSP00000503081.1:n.*337A>C
ENST00000676744.1:n.267A>C (LAMB1)
ENST00000676777.1:c.4421A>C (LAMB1)	ENSP00000504756.1:p.Glu1474Ala
ENST00000677101.1:c.*4057A>C (LAMB1)	ENSP00000503156.1:n.*4057A>C
ENST00000677144.1:c.*1240A>C (LAMB1)	ENSP00000503049.1:n.*1240A>C
ENST00000677485.1:n.5645A>C (LAMB1)
ENST00000677588.1:c.*652A>C (LAMB1)	ENSP00000502938.1:n.*652A>C
ENST00000677793.1:c.4109A>C (LAMB1)	ENSP00000504020.1:p.Glu1370Ala
ENST00000677801.1:c.*250A>C (LAMB1)	ENSP00000503438.1:n.*250A>C
ENST00000678232.1:n.4610A>C (LAMB1)
ENST00000678310.1:n.2590A>C (LAMB1)
ENST00000678698.1:c.*493A>C (LAMB1)	ENSP00000503198.1:n.*493A>C
ENST00000678704.1:c.*3003A>C (LAMB1)	ENSP00000504589.1:n.*3003A>C
ENST00000678892.1:c.*493A>C (LAMB1)	ENSP00000504841.1:n.*493A>C
ENST00000679200.1:c.*493A>C (LAMB1)	ENSP00000503498.1:n.*493A>C
ENST00000222399.10:c.4421A>C (LAMB1)	ENSP00000222399.6:p.Glu1474Ala
ENST00000393561.5:c.4493A>C (LAMB1)	ENSP00000377191.1:p.Glu1498Ala
ENST00000417551.5:c.*166T>G (DLD)	ENSP00000390667.1:n.*166T>G
ENST00000468518.1:n.480A>C (LAMB1)
ENST00000474380.1:n.658A>C (LAMB1)
NM_002291.2:c.4421A>C (LAMB1)	NP_002282.2:p.Glu1474Ala
XM_017012201.1:c.4493A>C (LAMB1)	XP_016867690.1:p.Glu1498Ala
XR_001744756.1:n.5340A>C (LAMB1)
NM_002291.3:c.4421A>C (LAMB1) MANE Select	NP_002282.2:p.Glu1474Ala