Canonical Allele Identifier: CA1732869462

Gene: LAMB1

Linked Data

• dbSNP Id: rs539202519

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107951388_107951389del , CM000669.2:g.107951388_107951389del	GRCh38
NC_000007.13:g.107591833_107591834del , CM000669.1:g.107591833_107591834del	GRCh37
NC_000007.12:g.107379069_107379070del	NCBI36
NG_023255.1:g.56977_56978del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222399.11:c.3295-61_3295-60del MANE Select	ENSP00000222399.6:n.3295-61_3295-60del
ENST00000393561.6:c.2884-61_2884-60del	ENSP00000377191.2:n.2884-61_2884-60del
ENST00000676574.1:c.3295-61_3295-60del	ENSP00000503081.1:n.3295-61_3295-60del
ENST00000676777.1:c.3295-61_3295-60del	ENSP00000504756.1:n.3295-61_3295-60del
ENST00000676920.1:c.2884-61_2884-60del	ENSP00000503814.1:n.2884-61_2884-60del
ENST00000677101.1:c.*2931-61_*2931-60del	ENSP00000503156.1:n.*2931-61_*2931-60del
ENST00000677144.1:c.*114-61_*114-60del	ENSP00000503049.1:n.*114-61_*114-60del
ENST00000677485.1:n.4519-61_4519-60del
ENST00000677588.1:c.3295-61_3295-60del	ENSP00000502938.1:n.3295-61_3295-60del
ENST00000677652.1:n.3484-61_3484-60del
ENST00000677793.1:c.3079+2147_3079+2148del	ENSP00000504020.1:n.3079+2147_3079+2148del
ENST00000677801.1:c.2884-61_2884-60del	ENSP00000503438.1:n.2884-61_2884-60del
ENST00000677994.1:n.3461-61_3461-60del
ENST00000678232.1:n.3484-61_3484-60del
ENST00000678266.1:n.3437-61_3437-60del
ENST00000678346.1:c.*2931-61_*2931-60del	ENSP00000504349.1:n.*2931-61_*2931-60del
ENST00000678698.1:c.2884-61_2884-60del	ENSP00000503198.1:n.2884-61_2884-60del
ENST00000678704.1:c.*1877-61_*1877-60del	ENSP00000504589.1:n.*1877-61_*1877-60del
ENST00000678892.1:c.3295-61_3295-60del	ENSP00000504841.1:n.3295-61_3295-60del
ENST00000679173.1:n.3484-61_3484-60del
ENST00000679200.1:c.2884-61_2884-60del	ENSP00000503498.1:n.2884-61_2884-60del
ENST00000679244.1:c.3295-61_3295-60del	ENSP00000504656.1:n.3295-61_3295-60del
ENST00000222399.10:c.3295-61_3295-60del	ENSP00000222399.6:n.3295-61_3295-60del
ENST00000393561.5:c.3367-61_3367-60del	ENSP00000377191.1:n.3367-61_3367-60del
ENST00000476039.1:n.336-61_336-60del
ENST00000479448.1:n.83-61_83-60del
NM_002291.2:c.3295-61_3295-60del	NP_002282.2:n.3295-61_3295-60del
XM_011516203.1:c.3295-61_3295-60del	XP_011514505.1:n.3295-61_3295-60del
XM_017012201.1:c.3367-61_3367-60del	XP_016867690.1:n.3367-61_3367-60del
XM_017012202.1:c.3367-61_3367-60del	XP_016867691.1:n.3367-61_3367-60del
XR_001744756.1:n.4098-61_4098-60del
NM_002291.3:c.3295-61_3295-60del MANE Select	NP_002282.2:n.3295-61_3295-60del