Canonical Allele Identifier: CA1732869509

Gene: LAMB1

Linked Data

• dbSNP Id: rs2033248008

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107951424_107951425dup , CM000669.2:g.107951424_107951425dup	GRCh38
NC_000007.13:g.107591869_107591870dup , CM000669.1:g.107591869_107591870dup	GRCh37
NC_000007.12:g.107379105_107379106dup	NCBI36
NG_023255.1:g.56935_56936dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222399.11:c.3295-103_3295-102dup MANE Select	ENSP00000222399.6:n.3295-103_3295-102dup
ENST00000393561.6:c.2884-103_2884-102dup	ENSP00000377191.2:n.2884-103_2884-102dup
ENST00000676574.1:c.3295-103_3295-102dup	ENSP00000503081.1:n.3295-103_3295-102dup
ENST00000676777.1:c.3295-103_3295-102dup	ENSP00000504756.1:n.3295-103_3295-102dup
ENST00000676920.1:c.2884-103_2884-102dup	ENSP00000503814.1:n.2884-103_2884-102dup
ENST00000677101.1:c.*2931-103_*2931-102dup	ENSP00000503156.1:n.*2931-103_*2931-102dup
ENST00000677144.1:c.*114-103_*114-102dup	ENSP00000503049.1:n.*114-103_*114-102dup
ENST00000677485.1:n.4519-103_4519-102dup
ENST00000677588.1:c.3295-103_3295-102dup	ENSP00000502938.1:n.3295-103_3295-102dup
ENST00000677652.1:n.3484-103_3484-102dup
ENST00000677793.1:c.3079+2105_3079+2106dup	ENSP00000504020.1:n.3079+2105_3079+2106dup
ENST00000677801.1:c.2884-103_2884-102dup	ENSP00000503438.1:n.2884-103_2884-102dup
ENST00000677994.1:n.3461-103_3461-102dup
ENST00000678232.1:n.3484-103_3484-102dup
ENST00000678266.1:n.3437-103_3437-102dup
ENST00000678346.1:c.*2931-103_*2931-102dup	ENSP00000504349.1:n.*2931-103_*2931-102dup
ENST00000678698.1:c.2884-103_2884-102dup	ENSP00000503198.1:n.2884-103_2884-102dup
ENST00000678704.1:c.*1877-103_*1877-102dup	ENSP00000504589.1:n.*1877-103_*1877-102dup
ENST00000678892.1:c.3295-103_3295-102dup	ENSP00000504841.1:n.3295-103_3295-102dup
ENST00000679173.1:n.3484-103_3484-102dup
ENST00000679200.1:c.2884-103_2884-102dup	ENSP00000503498.1:n.2884-103_2884-102dup
ENST00000679244.1:c.3295-103_3295-102dup	ENSP00000504656.1:n.3295-103_3295-102dup
ENST00000222399.10:c.3295-103_3295-102dup	ENSP00000222399.6:n.3295-103_3295-102dup
ENST00000393561.5:c.3367-103_3367-102dup	ENSP00000377191.1:n.3367-103_3367-102dup
ENST00000476039.1:n.336-103_336-102dup
ENST00000479448.1:n.83-103_83-102dup
NM_002291.2:c.3295-103_3295-102dup	NP_002282.2:n.3295-103_3295-102dup
XM_011516203.1:c.3295-103_3295-102dup	XP_011514505.1:n.3295-103_3295-102dup
XM_017012201.1:c.3367-103_3367-102dup	XP_016867690.1:n.3367-103_3367-102dup
XM_017012202.1:c.3367-103_3367-102dup	XP_016867691.1:n.3367-103_3367-102dup
XR_001744756.1:n.4098-103_4098-102dup
NM_002291.3:c.3295-103_3295-102dup MANE Select	NP_002282.2:n.3295-103_3295-102dup