Canonical Allele Identifier: CA457111247

Gene: LAMB1 DLD

Linked Data

• MyVariant Identifiers: chr7:g.107571886C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107931441C>T , CM000669.2:g.107931441C>T	GRCh38
NC_000007.13:g.107571886C>T , CM000669.1:g.107571886C>T	GRCh37
NC_000007.12:g.107359122C>T	NCBI36
NG_023255.1:g.76919G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222399.11:c.4452G>A (LAMB1) MANE Select	ENSP00000222399.6:p.Leu1484=
ENST00000393561.6:c.4041G>A (LAMB1)	ENSP00000377191.2:p.Leu1347=
ENST00000468518.2:n.2686G>A (LAMB1)
ENST00000468999.2:n.2600G>A (LAMB1)
ENST00000474380.2:n.1267G>A (LAMB1)
ENST00000676574.1:c.*368G>A (LAMB1)	ENSP00000503081.1:n.*368G>A
ENST00000676744.1:n.298G>A (LAMB1)
ENST00000676777.1:c.4452G>A (LAMB1)	ENSP00000504756.1:p.Leu1484=
ENST00000677101.1:c.*4088G>A (LAMB1)	ENSP00000503156.1:n.*4088G>A
ENST00000677144.1:c.*1271G>A (LAMB1)	ENSP00000503049.1:n.*1271G>A
ENST00000677485.1:n.5676G>A (LAMB1)
ENST00000677588.1:c.*683G>A (LAMB1)	ENSP00000502938.1:n.*683G>A
ENST00000677793.1:c.4140G>A (LAMB1)	ENSP00000504020.1:p.Leu1380=
ENST00000677801.1:c.*281G>A (LAMB1)	ENSP00000503438.1:n.*281G>A
ENST00000678232.1:n.4641G>A (LAMB1)
ENST00000678310.1:n.2621G>A (LAMB1)
ENST00000678698.1:c.*524G>A (LAMB1)	ENSP00000503198.1:n.*524G>A
ENST00000678704.1:c.*3034G>A (LAMB1)	ENSP00000504589.1:n.*3034G>A
ENST00000678892.1:c.*524G>A (LAMB1)	ENSP00000504841.1:n.*524G>A
ENST00000679200.1:c.*524G>A (LAMB1)	ENSP00000503498.1:n.*524G>A
ENST00000222399.10:c.4452G>A (LAMB1)	ENSP00000222399.6:p.Leu1484=
ENST00000393561.5:c.4524G>A (LAMB1)	ENSP00000377191.1:p.Leu1508=
ENST00000417551.5:c.*135C>T (DLD)	ENSP00000390667.1:n.*135C>T
ENST00000468518.1:n.511G>A (LAMB1)
ENST00000474380.1:n.689G>A (LAMB1)
NM_002291.2:c.4452G>A (LAMB1)	NP_002282.2:p.Leu1484=
XM_017012201.1:c.4524G>A (LAMB1)	XP_016867690.1:p.Leu1508=
XR_001744756.1:n.5371G>A (LAMB1)
NM_002291.3:c.4452G>A (LAMB1) MANE Select	NP_002282.2:p.Leu1484=