Canonical Allele Identifier: CA2578990490

Gene: LAMB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107951360del , CM000669.2:g.107951360del	GRCh38
NC_000007.13:g.107591805del , CM000669.1:g.107591805del	GRCh37
NC_000007.12:g.107379041del	NCBI36
NG_023255.1:g.57000del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222399.11:c.3295-38del MANE Select	ENSP00000222399.6:n.3295-38del
ENST00000393561.6:c.2884-38del	ENSP00000377191.2:n.2884-38del
ENST00000676574.1:c.3295-38del	ENSP00000503081.1:n.3295-38del
ENST00000676777.1:c.3295-38del	ENSP00000504756.1:n.3295-38del
ENST00000676920.1:c.2884-38del	ENSP00000503814.1:n.2884-38del
ENST00000677101.1:c.*2931-38del	ENSP00000503156.1:n.*2931-38del
ENST00000677144.1:c.*114-38del	ENSP00000503049.1:n.*114-38del
ENST00000677485.1:n.4519-38del
ENST00000677588.1:c.3295-38del	ENSP00000502938.1:n.3295-38del
ENST00000677652.1:n.3484-38del
ENST00000677793.1:c.3079+2170del	ENSP00000504020.1:n.3079+2170del
ENST00000677801.1:c.2884-38del	ENSP00000503438.1:n.2884-38del
ENST00000677994.1:n.3461-38del
ENST00000678232.1:n.3484-38del
ENST00000678266.1:n.3437-38del
ENST00000678346.1:c.*2931-38del	ENSP00000504349.1:n.*2931-38del
ENST00000678698.1:c.2884-38del	ENSP00000503198.1:n.2884-38del
ENST00000678704.1:c.*1877-38del	ENSP00000504589.1:n.*1877-38del
ENST00000678892.1:c.3295-38del	ENSP00000504841.1:n.3295-38del
ENST00000679173.1:n.3484-38del
ENST00000679200.1:c.2884-38del	ENSP00000503498.1:n.2884-38del
ENST00000679244.1:c.3295-38del	ENSP00000504656.1:n.3295-38del
ENST00000222399.10:c.3295-38del	ENSP00000222399.6:n.3295-38del
ENST00000393561.5:c.3367-38del	ENSP00000377191.1:n.3367-38del
ENST00000476039.1:n.336-38del
ENST00000479448.1:n.83-38del
NM_002291.2:c.3295-38del	NP_002282.2:n.3295-38del
XM_011516203.1:c.3295-38del	XP_011514505.1:n.3295-38del
XM_017012201.1:c.3367-38del	XP_016867690.1:n.3367-38del
XM_017012202.1:c.3367-38del	XP_016867691.1:n.3367-38del
XR_001744756.1:n.4098-38del
NM_002291.3:c.3295-38del MANE Select	NP_002282.2:n.3295-38del