Canonical Allele Identifier: CA368864285

Gene: LAMB1 DLD

Linked Data

• MyVariant Identifiers: chr7:g.107571931T>G (hg19) ; chr7:g.107931486T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107931486T>G , CM000669.2:g.107931486T>G	GRCh38
NC_000007.13:g.107571931T>G , CM000669.1:g.107571931T>G	GRCh37
NC_000007.12:g.107359167T>G	NCBI36
NG_023255.1:g.76874A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222399.11:c.4407A>C (LAMB1) MANE Select	ENSP00000222399.6:p.Lys1469Asn
ENST00000393561.6:c.3996A>C (LAMB1)	ENSP00000377191.2:p.Lys1332Asn
ENST00000468518.2:n.2641A>C (LAMB1)
ENST00000468999.2:n.2555A>C (LAMB1)
ENST00000474380.2:n.1222A>C (LAMB1)
ENST00000676574.1:c.*323A>C (LAMB1)	ENSP00000503081.1:n.*323A>C
ENST00000676744.1:n.253A>C (LAMB1)
ENST00000676777.1:c.4407A>C (LAMB1)	ENSP00000504756.1:p.Lys1469Asn
ENST00000677101.1:c.*4043A>C (LAMB1)	ENSP00000503156.1:n.*4043A>C
ENST00000677144.1:c.*1226A>C (LAMB1)	ENSP00000503049.1:n.*1226A>C
ENST00000677485.1:n.5631A>C (LAMB1)
ENST00000677588.1:c.*638A>C (LAMB1)	ENSP00000502938.1:n.*638A>C
ENST00000677793.1:c.4095A>C (LAMB1)	ENSP00000504020.1:p.Lys1365Asn
ENST00000677801.1:c.*236A>C (LAMB1)	ENSP00000503438.1:n.*236A>C
ENST00000678232.1:n.4596A>C (LAMB1)
ENST00000678310.1:n.2576A>C (LAMB1)
ENST00000678698.1:c.*479A>C (LAMB1)	ENSP00000503198.1:n.*479A>C
ENST00000678704.1:c.*2989A>C (LAMB1)	ENSP00000504589.1:n.*2989A>C
ENST00000678892.1:c.*479A>C (LAMB1)	ENSP00000504841.1:n.*479A>C
ENST00000679200.1:c.*479A>C (LAMB1)	ENSP00000503498.1:n.*479A>C
ENST00000222399.10:c.4407A>C (LAMB1)	ENSP00000222399.6:p.Lys1469Asn
ENST00000393561.5:c.4479A>C (LAMB1)	ENSP00000377191.1:p.Lys1493Asn
ENST00000417551.5:c.*180T>G (DLD)	ENSP00000390667.1:n.*180T>G
ENST00000468518.1:n.466A>C (LAMB1)
ENST00000474380.1:n.644A>C (LAMB1)
NM_002291.2:c.4407A>C (LAMB1)	NP_002282.2:p.Lys1469Asn
XM_017012201.1:c.4479A>C (LAMB1)	XP_016867690.1:p.Lys1493Asn
XR_001744756.1:n.5326A>C (LAMB1)
NM_002291.3:c.4407A>C (LAMB1) MANE Select	NP_002282.2:p.Lys1469Asn