Canonical Allele Identifier: CA645544108
Gene: BRAF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753340_140753341insTAT , CM000669.2:g.140753340_140753341insTAT GRCh38
NC_000007.13:g.140453140_140453141insTAT , CM000669.1:g.140453140_140453141insTAT GRCh37
NC_000007.12:g.140099609_140099610insTAT NCBI36
NG_007873.3:g.176425_176426insTAA , LRG_299:g.176425_176426insTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1795_1796insTAA MANE Select ENSP00000493543.1:p.Ala598_Thr599insIle
ENST00000288602.11:c.1915_1916insTAA ENSP00000288602.7:p.Ala638_Thr639insIle
ENST00000479537.6:c.465_466insTAA
ENST00000496384.7:c.1795_1796insTAA ENSP00000419060.2:p.Ala598_Thr599insIle
ENST00000497784.2:c.*1245_*1246insTAA ENSP00000420119.2:n.*1245_*1246insTAA
ENST00000642228.1:c.*873_*874insTAA ENSP00000493678.1:n.*873_*874insTAA
ENST00000642875.1:n.1259-3922_1259-3921insTAA
ENST00000644120.1:n.2185_2186insTAA
ENST00000644650.1:c.891_892insTAA
ENST00000644905.1:n.2677_2678insTAA
ENST00000644969.2:c.1915_1916insTAA MANE Plus Clinical ENSP00000496776.1:p.Ala638_Thr639insIle
ENST00000646730.1:c.*371_*372insTAA ENSP00000494784.1:n.*371_*372insTAA
ENST00000646891.1:c.1795_1796insTAA ENSP00000493543.1:p.Ala598_Thr599insIle
ENST00000647434.1:c.738-3922_738-3921insTAA ENSP00000495132.1:n.738-3922_738-3921insTAA
ENST00000288602.10:c.1795_1796insTAA ENSP00000288602.6:p.Ala598_Thr599insIle
ENST00000479537.5:c.79_80insTAA ENSP00000418033.1:p.Ala26_Thr27insIle
ENST00000496384.6:c.618_619insTAA
ENST00000497784.1:c.1830_1831insTAA ENSP00000420119.1:n.1830_1831insTAA
NM_004333.4:c.1795_1796insTAA , LRG_299t1:c.1795_1796insTAA NP_004324.2:p.Ala598_Thr599insIle
XM_005250045.1:c.1795_1796insTAA XP_005250102.1:p.Ala598_Thr599insIle
XM_005250046.1:c.1795_1796insTAA XP_005250103.1:p.Ala598_Thr599insIle
XM_011516529.1:c.1795_1796insTAA XP_011514831.1:p.Ala598_Thr599insIle
XM_011516530.1:c.1695-3922_1695-3921insTAA XP_011514832.1:n.1695-3922_1695-3921insTAA
XR_242190.1:n.1803_1804insTAA
XR_927520.1:n.1803_1804insTAA
XR_927521.1:n.1803_1804insTAA
XR_927522.1:n.1703-3922_1703-3921insTAA
XR_927523.1:n.1703-3922_1703-3921insTAA
NM_001354609.1:c.1795_1796insTAA NP_001341538.1:p.Ala598_Thr599insIle
NM_004333.5:c.1795_1796insTAA NP_004324.2:p.Ala598_Thr599insIle
NR_148928.1:n.2893_2894insTAA
XM_017012558.1:c.1915_1916insTAA XP_016868047.1:p.Ala638_Thr639insIle
XM_017012559.1:c.1915_1916insTAA XP_016868048.1:p.Ala638_Thr639insIle
XR_001744857.1:n.1923_1924insTAA
XR_001744858.1:n.1823-3922_1823-3921insTAA
NM_001354609.2:c.1795_1796insTAA NP_001341538.1:p.Ala598_Thr599insIle
NM_001374244.1:c.1915_1916insTAA NP_001361173.1:p.Ala638_Thr639insIle
NM_001374258.1:c.1915_1916insTAA MANE Plus Clinical NP_001361187.1:p.Ala638_Thr639insIle
NM_004333.6:c.1795_1796insTAA MANE Select NP_004324.2:p.Ala598_Thr599insIle
NM_001378467.1:c.1804_1805insTAA NP_001365396.1:p.Ala601_Thr602insIle
NM_001378468.1:c.1795_1796insTAA NP_001365397.1:p.Ala598_Thr599insIle
NM_001378469.1:c.1729_1730insTAA NP_001365398.1:p.Ala576_Thr577insIle
NM_001378470.1:c.1693_1694insTAA NP_001365399.1:p.Ala564_Thr565insIle
NM_001378471.1:c.1684_1685insTAA NP_001365400.1:p.Ala561_Thr562insIle
NM_001378472.1:c.1639_1640insTAA NP_001365401.1:p.Ala546_Thr547insIle
NM_001378473.1:c.1639_1640insTAA NP_001365402.1:p.Ala546_Thr547insIle
NM_001378474.1:c.1795_1796insTAA NP_001365403.1:p.Ala598_Thr599insIle
NM_001378475.1:c.1531_1532insTAA NP_001365404.1:p.Ala510_Thr511insIle