Canonical Allele Identifier: CA457109994
Gene: LAMB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.107613447A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107973002A>G , CM000669.2:g.107973002A>G GRCh38
NC_000007.13:g.107613447A>G , CM000669.1:g.107613447A>G GRCh37
NC_000007.12:g.107400683A>G NCBI36
NG_023255.1:g.35358T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222399.11:c.1552T>C MANE Select ENSP00000222399.6:p.Leu518=
ENST00000393561.6:c.1141T>C ENSP00000377191.2:p.Leu381=
ENST00000439976.6:c.1810T>C ENSP00000412686.2:p.Leu604=
ENST00000676574.1:c.1552T>C ENSP00000503081.1:p.Leu518=
ENST00000676777.1:c.1552T>C ENSP00000504756.1:p.Leu518=
ENST00000676920.1:c.1141T>C ENSP00000503814.1:p.Leu381=
ENST00000677101.1:c.*1188T>C ENSP00000503156.1:n.*1188T>C
ENST00000677144.1:c.1552T>C ENSP00000503049.1:p.Leu518=
ENST00000677485.1:n.2776T>C
ENST00000677588.1:c.1552T>C ENSP00000502938.1:p.Leu518=
ENST00000677652.1:n.1741T>C
ENST00000677734.1:n.1741T>C
ENST00000677793.1:c.1552T>C ENSP00000504020.1:p.Leu518=
ENST00000677801.1:c.1141T>C ENSP00000503438.1:p.Leu381=
ENST00000677994.1:n.1718T>C
ENST00000678232.1:n.1741T>C
ENST00000678266.1:n.1694T>C
ENST00000678346.1:c.*1188T>C ENSP00000504349.1:n.*1188T>C
ENST00000678698.1:c.1141T>C ENSP00000503198.1:p.Leu381=
ENST00000678704.1:c.*134T>C ENSP00000504589.1:n.*134T>C
ENST00000678892.1:c.1552T>C ENSP00000504841.1:p.Leu518=
ENST00000679173.1:n.1741T>C
ENST00000679200.1:c.1141T>C ENSP00000503498.1:p.Leu381=
ENST00000679244.1:c.1552T>C ENSP00000504656.1:p.Leu518=
ENST00000222399.10:c.1552T>C ENSP00000222399.6:p.Leu518=
ENST00000393560.5:c.1552T>C ENSP00000377190.1:p.Leu518=
ENST00000393561.5:c.1624T>C ENSP00000377191.1:p.Leu542=
NM_002291.2:c.1552T>C NP_002282.2:p.Leu518=
XM_011516203.1:c.1552T>C XP_011514505.1:p.Leu518=
XM_017012201.1:c.1624T>C XP_016867690.1:p.Leu542=
XM_017012202.1:c.1624T>C XP_016867691.1:p.Leu542=
XR_001744756.1:n.2355T>C
NM_002291.3:c.1552T>C MANE Select NP_002282.2:p.Leu518=