Canonical Allele Identifier: CA4435327

Gene: LAMB1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107940394A>G , CM000669.2:g.107940394A>G	GRCh38
NC_000007.13:g.107580839A>G , CM000669.1:g.107580839A>G	GRCh37
NC_000007.12:g.107368075A>G	NCBI36
NG_023255.1:g.67966T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222399.11:c.3392-36T>C MANE Select	ENSP00000222399.6:n.3392-36T>C
ENST00000393561.6:c.2981-36T>C	ENSP00000377191.2:n.2981-36T>C
ENST00000468999.2:n.1409T>C
ENST00000474380.2:n.171T>C
ENST00000676574.1:c.3392-36T>C	ENSP00000503081.1:n.3392-36T>C
ENST00000676777.1:c.3392-36T>C	ENSP00000504756.1:n.3392-36T>C
ENST00000677101.1:c.*3028-36T>C	ENSP00000503156.1:n.*3028-36T>C
ENST00000677144.1:c.*211-36T>C	ENSP00000503049.1:n.*211-36T>C
ENST00000677485.1:n.4616-36T>C
ENST00000677588.1:c.3392-3117T>C	ENSP00000502938.1:n.3392-3117T>C
ENST00000677652.1:n.3581-36T>C
ENST00000677793.1:c.3080-36T>C	ENSP00000504020.1:n.3080-36T>C
ENST00000677801.1:c.2981-36T>C	ENSP00000503438.1:n.2981-36T>C
ENST00000678232.1:n.3581-36T>C
ENST00000678310.1:n.1409T>C
ENST00000678346.1:c.*3028-3117T>C	ENSP00000504349.1:n.*3028-3117T>C
ENST00000678698.1:c.2981-36T>C	ENSP00000503198.1:n.2981-36T>C
ENST00000678704.1:c.*1974-36T>C	ENSP00000504589.1:n.*1974-36T>C
ENST00000678892.1:c.3392-36T>C	ENSP00000504841.1:n.3392-36T>C
ENST00000679173.1:n.3581-3117T>C
ENST00000679200.1:c.2981-36T>C	ENSP00000503498.1:n.2981-36T>C
ENST00000222399.10:c.3392-36T>C	ENSP00000222399.6:n.3392-36T>C
ENST00000393561.5:c.3464-36T>C	ENSP00000377191.1:n.3464-36T>C
ENST00000468999.1:n.171T>C
NM_002291.2:c.3392-36T>C	NP_002282.2:n.3392-36T>C
XM_011516203.1:c.3392-36T>C	XP_011514505.1:n.3392-36T>C
XM_017012201.1:c.3464-36T>C	XP_016867690.1:n.3464-36T>C
XR_001744756.1:n.4195-36T>C
NM_002291.3:c.3392-36T>C MANE Select	NP_002282.2:n.3392-36T>C