Canonical Allele Identifier: CA891842034
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753345_140753347dup , CM000669.2:g.140753345_140753347dup GRCh38
NC_000007.13:g.140453145_140453147dup , CM000669.1:g.140453145_140453147dup GRCh37
NC_000007.12:g.140099614_140099616dup NCBI36
NG_007873.3:g.176418_176420dup , LRG_299:g.176418_176420dup

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1788_1790dup MANE Select ENSP00000493543.1:p.Leu597_Ala598insLeu
ENST00000288602.11:c.1908_1910dup ENSP00000288602.7:p.Leu637_Ala638insLeu
ENST00000479537.6:c.458_460dup
ENST00000496384.7:c.1788_1790dup ENSP00000419060.2:p.Leu597_Ala598insLeu
ENST00000497784.2:c.*1238_*1240dup ENSP00000420119.2:n.*1238_*1240dup
ENST00000642228.1:c.*866_*868dup ENSP00000493678.1:n.*866_*868dup
ENST00000642875.1:n.1259-3929_1259-3927dup
ENST00000644120.1:n.2178_2180dup
ENST00000644650.1:c.884_886dup
ENST00000644905.1:n.2670_2672dup
ENST00000644969.2:c.1908_1910dup MANE Plus Clinical ENSP00000496776.1:p.Leu637_Ala638insLeu
ENST00000646730.1:c.*364_*366dup ENSP00000494784.1:n.*364_*366dup
ENST00000646891.1:c.1788_1790dup ENSP00000493543.1:p.Leu597_Ala598insLeu
ENST00000647434.1:c.738-3929_738-3927dup ENSP00000495132.1:n.738-3929_738-3927dup
ENST00000288602.10:c.1788_1790dup ENSP00000288602.6:p.Leu597_Ala598insLeu
ENST00000479537.5:c.72_74dup ENSP00000418033.1:p.Leu25_Ala26insLeu
ENST00000496384.6:c.611_613dup
ENST00000497784.1:c.1823_1825dup ENSP00000420119.1:n.1823_1825dup
NM_004333.4:c.1788_1790dup , LRG_299t1:c.1788_1790dup NP_004324.2:p.Leu597_Ala598insLeu
XM_005250045.1:c.1788_1790dup XP_005250102.1:p.Leu597_Ala598insLeu
XM_005250046.1:c.1788_1790dup XP_005250103.1:p.Leu597_Ala598insLeu
XM_011516529.1:c.1788_1790dup XP_011514831.1:p.Leu597_Ala598insLeu
XM_011516530.1:c.1695-3929_1695-3927dup XP_011514832.1:n.1695-3929_1695-3927dup
XR_242190.1:n.1796_1798dup
XR_927520.1:n.1796_1798dup
XR_927521.1:n.1796_1798dup
XR_927522.1:n.1703-3929_1703-3927dup
XR_927523.1:n.1703-3929_1703-3927dup
NM_001354609.1:c.1788_1790dup NP_001341538.1:p.Leu597_Ala598insLeu
NM_004333.5:c.1788_1790dup NP_004324.2:p.Leu597_Ala598insLeu
NR_148928.1:n.2886_2888dup
XM_017012558.1:c.1908_1910dup XP_016868047.1:p.Leu637_Ala638insLeu
XM_017012559.1:c.1908_1910dup XP_016868048.1:p.Leu637_Ala638insLeu
XR_001744857.1:n.1916_1918dup
XR_001744858.1:n.1823-3929_1823-3927dup
NM_001354609.2:c.1788_1790dup NP_001341538.1:p.Leu597_Ala598insLeu
NM_001374244.1:c.1908_1910dup NP_001361173.1:p.Leu637_Ala638insLeu
NM_001374258.1:c.1908_1910dup MANE Plus Clinical NP_001361187.1:p.Leu637_Ala638insLeu
NM_004333.6:c.1788_1790dup MANE Select NP_004324.2:p.Leu597_Ala598insLeu
NM_001378467.1:c.1797_1799dup NP_001365396.1:p.Leu600_Ala601insLeu
NM_001378468.1:c.1788_1790dup NP_001365397.1:p.Leu597_Ala598insLeu
NM_001378469.1:c.1722_1724dup NP_001365398.1:p.Leu575_Ala576insLeu
NM_001378470.1:c.1686_1688dup NP_001365399.1:p.Leu563_Ala564insLeu
NM_001378471.1:c.1677_1679dup NP_001365400.1:p.Leu560_Ala561insLeu
NM_001378472.1:c.1632_1634dup NP_001365401.1:p.Leu545_Ala546insLeu
NM_001378473.1:c.1632_1634dup NP_001365402.1:p.Leu545_Ala546insLeu
NM_001378474.1:c.1788_1790dup NP_001365403.1:p.Leu597_Ala598insLeu
NM_001378475.1:c.1524_1526dup NP_001365404.1:p.Leu509_Ala510insLeu