Canonical Allele Identifier: CA2850447116
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753345_140753346delinsGC , CM000669.2:g.140753345_140753346delinsGC GRCh38
NC_000007.13:g.140453145_140453146delinsGC , CM000669.1:g.140453145_140453146delinsGC GRCh37
NC_000007.12:g.140099614_140099615delinsGC NCBI36
NG_007873.3:g.176419_176420delinsGC , LRG_299:g.176419_176420delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1789_1790delinsGC MANE Select ENSP00000493543.1:p.Leu597Ala
ENST00000288602.11:c.1909_1910delinsGC ENSP00000288602.7:p.Leu637Ala
ENST00000479537.6:c.459_460delinsGC
ENST00000496384.7:c.1789_1790delinsGC ENSP00000419060.2:p.Leu597Ala
ENST00000497784.2:c.*1239_*1240delinsGC ENSP00000420119.2:n.*1239_*1240delinsGC
ENST00000642228.1:c.*867_*868delinsGC ENSP00000493678.1:n.*867_*868delinsGC
ENST00000642875.1:n.1259-3928_1259-3927delinsGC
ENST00000644120.1:n.2179_2180delinsGC
ENST00000644650.1:c.885_886delinsGC
ENST00000644905.1:n.2671_2672delinsGC
ENST00000644969.2:c.1909_1910delinsGC MANE Plus Clinical ENSP00000496776.1:p.Leu637Ala
ENST00000646730.1:c.*365_*366delinsGC ENSP00000494784.1:n.*365_*366delinsGC
ENST00000646891.1:c.1789_1790delinsGC ENSP00000493543.1:p.Leu597Ala
ENST00000647434.1:c.738-3928_738-3927delinsGC ENSP00000495132.1:n.738-3928_738-3927delinsGC
ENST00000288602.10:c.1789_1790delinsGC ENSP00000288602.6:p.Leu597Ala
ENST00000479537.5:c.73_74delinsGC ENSP00000418033.1:p.Leu25Ala
ENST00000496384.6:c.612_613delinsGC
ENST00000497784.1:c.1824_1825delinsGC ENSP00000420119.1:n.1824_1825delinsGC
NM_004333.4:c.1789_1790delinsGC , LRG_299t1:c.1789_1790delinsGC NP_004324.2:p.Leu597Ala
XM_005250045.1:c.1789_1790delinsGC XP_005250102.1:p.Leu597Ala
XM_005250046.1:c.1789_1790delinsGC XP_005250103.1:p.Leu597Ala
XM_011516529.1:c.1789_1790delinsGC XP_011514831.1:p.Leu597Ala
XM_011516530.1:c.1695-3928_1695-3927delinsGC XP_011514832.1:n.1695-3928_1695-3927delinsGC
XR_242190.1:n.1797_1798delinsGC
XR_927520.1:n.1797_1798delinsGC
XR_927521.1:n.1797_1798delinsGC
XR_927522.1:n.1703-3928_1703-3927delinsGC
XR_927523.1:n.1703-3928_1703-3927delinsGC
NM_001354609.1:c.1789_1790delinsGC NP_001341538.1:p.Leu597Ala
NM_004333.5:c.1789_1790delinsGC NP_004324.2:p.Leu597Ala
NR_148928.1:n.2887_2888delinsGC
XM_017012558.1:c.1909_1910delinsGC XP_016868047.1:p.Leu637Ala
XM_017012559.1:c.1909_1910delinsGC XP_016868048.1:p.Leu637Ala
XR_001744857.1:n.1917_1918delinsGC
XR_001744858.1:n.1823-3928_1823-3927delinsGC
NM_001354609.2:c.1789_1790delinsGC NP_001341538.1:p.Leu597Ala
NM_001374244.1:c.1909_1910delinsGC NP_001361173.1:p.Leu637Ala
NM_001374258.1:c.1909_1910delinsGC MANE Plus Clinical NP_001361187.1:p.Leu637Ala
NM_004333.6:c.1789_1790delinsGC MANE Select NP_004324.2:p.Leu597Ala
NM_001378467.1:c.1798_1799delinsGC NP_001365396.1:p.Leu600Ala
NM_001378468.1:c.1789_1790delinsGC NP_001365397.1:p.Leu597Ala
NM_001378469.1:c.1723_1724delinsGC NP_001365398.1:p.Leu575Ala
NM_001378470.1:c.1687_1688delinsGC NP_001365399.1:p.Leu563Ala
NM_001378471.1:c.1678_1679delinsGC NP_001365400.1:p.Leu560Ala
NM_001378472.1:c.1633_1634delinsGC NP_001365401.1:p.Leu545Ala
NM_001378473.1:c.1633_1634delinsGC NP_001365402.1:p.Leu545Ala
NM_001378474.1:c.1789_1790delinsGC NP_001365403.1:p.Leu597Ala
NM_001378475.1:c.1525_1526delinsGC NP_001365404.1:p.Leu509Ala