Canonical Allele Identifier: CA2777362144

Gene: LAMB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107951432_107951433del , CM000669.2:g.107951432_107951433del	GRCh38
NC_000007.13:g.107591877_107591878del , CM000669.1:g.107591877_107591878del	GRCh37
NC_000007.12:g.107379113_107379114del	NCBI36
NG_023255.1:g.56927_56928del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222399.11:c.3295-111_3295-110del MANE Select	ENSP00000222399.6:n.3295-111_3295-110del
ENST00000393561.6:c.2884-111_2884-110del	ENSP00000377191.2:n.2884-111_2884-110del
ENST00000676574.1:c.3295-111_3295-110del	ENSP00000503081.1:n.3295-111_3295-110del
ENST00000676777.1:c.3295-111_3295-110del	ENSP00000504756.1:n.3295-111_3295-110del
ENST00000676920.1:c.2884-111_2884-110del	ENSP00000503814.1:n.2884-111_2884-110del
ENST00000677101.1:c.*2931-111_*2931-110del	ENSP00000503156.1:n.*2931-111_*2931-110del
ENST00000677144.1:c.*114-111_*114-110del	ENSP00000503049.1:n.*114-111_*114-110del
ENST00000677485.1:n.4519-111_4519-110del
ENST00000677588.1:c.3295-111_3295-110del	ENSP00000502938.1:n.3295-111_3295-110del
ENST00000677652.1:n.3484-111_3484-110del
ENST00000677793.1:c.3079+2097_3079+2098del	ENSP00000504020.1:n.3079+2097_3079+2098del
ENST00000677801.1:c.2884-111_2884-110del	ENSP00000503438.1:n.2884-111_2884-110del
ENST00000677994.1:n.3461-111_3461-110del
ENST00000678232.1:n.3484-111_3484-110del
ENST00000678266.1:n.3437-111_3437-110del
ENST00000678346.1:c.*2931-111_*2931-110del	ENSP00000504349.1:n.*2931-111_*2931-110del
ENST00000678698.1:c.2884-111_2884-110del	ENSP00000503198.1:n.2884-111_2884-110del
ENST00000678704.1:c.*1877-111_*1877-110del	ENSP00000504589.1:n.*1877-111_*1877-110del
ENST00000678892.1:c.3295-111_3295-110del	ENSP00000504841.1:n.3295-111_3295-110del
ENST00000679173.1:n.3484-111_3484-110del
ENST00000679200.1:c.2884-111_2884-110del	ENSP00000503498.1:n.2884-111_2884-110del
ENST00000679244.1:c.3295-111_3295-110del	ENSP00000504656.1:n.3295-111_3295-110del
ENST00000222399.10:c.3295-111_3295-110del	ENSP00000222399.6:n.3295-111_3295-110del
ENST00000393561.5:c.3367-111_3367-110del	ENSP00000377191.1:n.3367-111_3367-110del
ENST00000476039.1:n.336-111_336-110del
ENST00000479448.1:n.83-111_83-110del
NM_002291.2:c.3295-111_3295-110del	NP_002282.2:n.3295-111_3295-110del
XM_011516203.1:c.3295-111_3295-110del	XP_011514505.1:n.3295-111_3295-110del
XM_017012201.1:c.3367-111_3367-110del	XP_016867690.1:n.3367-111_3367-110del
XM_017012202.1:c.3367-111_3367-110del	XP_016867691.1:n.3367-111_3367-110del
XR_001744756.1:n.4098-111_4098-110del
NM_002291.3:c.3295-111_3295-110del MANE Select	NP_002282.2:n.3295-111_3295-110del