Canonical Allele Identifier: CA368864067

Gene: LAMB1 DLD

Linked Data

• MyVariant Identifiers: chr7:g.107571876C>G (hg19) ; chr7:g.107931431C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107931431C>G , CM000669.2:g.107931431C>G	GRCh38
NC_000007.13:g.107571876C>G , CM000669.1:g.107571876C>G	GRCh37
NC_000007.12:g.107359112C>G	NCBI36
NG_023255.1:g.76929G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222399.11:c.4462G>C (LAMB1) MANE Select	ENSP00000222399.6:p.Ala1488Pro
ENST00000393561.6:c.4051G>C (LAMB1)	ENSP00000377191.2:p.Ala1351Pro
ENST00000468518.2:n.2696G>C (LAMB1)
ENST00000468999.2:n.2610G>C (LAMB1)
ENST00000474380.2:n.1277G>C (LAMB1)
ENST00000676574.1:c.*378G>C (LAMB1)	ENSP00000503081.1:n.*378G>C
ENST00000676744.1:n.308G>C (LAMB1)
ENST00000676777.1:c.4462G>C (LAMB1)	ENSP00000504756.1:p.Ala1488Pro
ENST00000677101.1:c.*4098G>C (LAMB1)	ENSP00000503156.1:n.*4098G>C
ENST00000677144.1:c.*1281G>C (LAMB1)	ENSP00000503049.1:n.*1281G>C
ENST00000677485.1:n.5686G>C (LAMB1)
ENST00000677588.1:c.*693G>C (LAMB1)	ENSP00000502938.1:n.*693G>C
ENST00000677793.1:c.4150G>C (LAMB1)	ENSP00000504020.1:p.Ala1384Pro
ENST00000677801.1:c.*291G>C (LAMB1)	ENSP00000503438.1:n.*291G>C
ENST00000678232.1:n.4651G>C (LAMB1)
ENST00000678310.1:n.2631G>C (LAMB1)
ENST00000678698.1:c.*534G>C (LAMB1)	ENSP00000503198.1:n.*534G>C
ENST00000678704.1:c.*3044G>C (LAMB1)	ENSP00000504589.1:n.*3044G>C
ENST00000678892.1:c.*534G>C (LAMB1)	ENSP00000504841.1:n.*534G>C
ENST00000679200.1:c.*534G>C (LAMB1)	ENSP00000503498.1:n.*534G>C
ENST00000222399.10:c.4462G>C (LAMB1)	ENSP00000222399.6:p.Ala1488Pro
ENST00000393561.5:c.4534G>C (LAMB1)	ENSP00000377191.1:p.Ala1512Pro
ENST00000417551.5:c.*125C>G (DLD)	ENSP00000390667.1:n.*125C>G
ENST00000468518.1:n.521G>C (LAMB1)
ENST00000474380.1:n.699G>C (LAMB1)
NM_002291.2:c.4462G>C (LAMB1)	NP_002282.2:p.Ala1488Pro
XM_017012201.1:c.4534G>C (LAMB1)	XP_016867690.1:p.Ala1512Pro
XR_001744756.1:n.5381G>C (LAMB1)
NM_002291.3:c.4462G>C (LAMB1) MANE Select	NP_002282.2:p.Ala1488Pro