Canonical Allele Identifier: CA645544103

Gene: BRAF

Linked Data

• COSMIC: COSM33780

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753337_140753339delinsAAGCTA , CM000669.2:g.140753337_140753339delinsAAGCTA	GRCh38
NC_000007.13:g.140453137_140453139delinsAAGCTA , CM000669.1:g.140453137_140453139delinsAAGCTA	GRCh37
NC_000007.12:g.140099606_140099608delinsAAGCTA	NCBI36
NG_007873.3:g.176426_176428delinsTAGCTT , LRG_299:g.176426_176428delinsTAGCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1796_1798delinsTAGCTT MANE Select	ENSP00000493543.1:p.Thr599_Val600delinsIl...
ENST00000288602.11:c.1916_1918delinsTAGCTT	ENSP00000288602.7:p.Thr639_Val640delinsIl...
ENST00000479537.6:c.466_468delinsTAGCTT
ENST00000496384.7:c.1796_1798delinsTAGCTT	ENSP00000419060.2:p.Thr599_Val600delinsIl...
ENST00000497784.2:c.*1246_*1248delinsTAGCTT	ENSP00000420119.2:n.*1246_*1248delinsTAGC...
ENST00000642228.1:c.*874_*876delinsTAGCTT	ENSP00000493678.1:n.*874_*876delinsTAGCTT...
ENST00000642875.1:n.1259-3921_1259-3919delinsTAGCTT
ENST00000644120.1:n.2186_2188delinsTAGCTT
ENST00000644650.1:c.892_894delinsTAGCTT
ENST00000644905.1:n.2678_2680delinsTAGCTT
ENST00000644969.2:c.1916_1918delinsTAGCTT MANE Plus Clinical	ENSP00000496776.1:p.Thr639_Val640delinsIl...
ENST00000646730.1:c.*372_*374delinsTAGCTT	ENSP00000494784.1:n.*372_*374delinsTAGCTT...
ENST00000646891.1:c.1796_1798delinsTAGCTT	ENSP00000493543.1:p.Thr599_Val600delinsIl...
ENST00000647434.1:c.738-3921_738-3919delinsTAGCTT	ENSP00000495132.1:n.738-3921_738-3919deli...
ENST00000288602.10:c.1796_1798delinsTAGCTT	ENSP00000288602.6:p.Thr599_Val600delinsIl...
ENST00000479537.5:c.80_82delinsTAGCTT	ENSP00000418033.1:p.Thr27_Val28delinsIleA...
ENST00000496384.6:c.619_621delinsTAGCTT
ENST00000497784.1:c.1831_1833delinsTAGCTT	ENSP00000420119.1:n.1831_1833delinsTAGCTT...
NM_004333.4:c.1796_1798delinsTAGCTT , LRG_299t1:c.1796_1798delinsTAGCTT	NP_004324.2:p.Thr599_Val600delinsIleAlaLe...
XM_005250045.1:c.1796_1798delinsTAGCTT	XP_005250102.1:p.Thr599_Val600delinsIleAl...
XM_005250046.1:c.1796_1798delinsTAGCTT	XP_005250103.1:p.Thr599_Val600delinsIleAl...
XM_011516529.1:c.1796_1798delinsTAGCTT	XP_011514831.1:p.Thr599_Val600delinsIleAl...
XM_011516530.1:c.1695-3921_1695-3919delinsTAGCTT	XP_011514832.1:n.1695-3921_1695-3919delin...
XR_242190.1:n.1804_1806delinsTAGCTT
XR_927520.1:n.1804_1806delinsTAGCTT
XR_927521.1:n.1804_1806delinsTAGCTT
XR_927522.1:n.1703-3921_1703-3919delinsTAGCTT
XR_927523.1:n.1703-3921_1703-3919delinsTAGCTT
NM_001354609.1:c.1796_1798delinsTAGCTT	NP_001341538.1:p.Thr599_Val600delinsIleAl...
NM_004333.5:c.1796_1798delinsTAGCTT	NP_004324.2:p.Thr599_Val600delinsIleAlaLe...
NR_148928.1:n.2894_2896delinsTAGCTT
XM_017012558.1:c.1916_1918delinsTAGCTT	XP_016868047.1:p.Thr639_Val640delinsIleAl...
XM_017012559.1:c.1916_1918delinsTAGCTT	XP_016868048.1:p.Thr639_Val640delinsIleAl...
XR_001744857.1:n.1924_1926delinsTAGCTT
XR_001744858.1:n.1823-3921_1823-3919delinsTAGCTT
NM_001354609.2:c.1796_1798delinsTAGCTT	NP_001341538.1:p.Thr599_Val600delinsIleAl...
NM_001374244.1:c.1916_1918delinsTAGCTT	NP_001361173.1:p.Thr639_Val640delinsIleAl...
NM_001374258.1:c.1916_1918delinsTAGCTT MANE Plus Clinical	NP_001361187.1:p.Thr639_Val640delinsIleAl...
NM_004333.6:c.1796_1798delinsTAGCTT MANE Select	NP_004324.2:p.Thr599_Val600delinsIleAlaLe...
NM_001378467.1:c.1805_1807delinsTAGCTT	NP_001365396.1:p.Thr602_Val603delinsIleAl...
NM_001378468.1:c.1796_1798delinsTAGCTT	NP_001365397.1:p.Thr599_Val600delinsIleAl...
NM_001378469.1:c.1730_1732delinsTAGCTT	NP_001365398.1:p.Thr577_Val578delinsIleAl...
NM_001378470.1:c.1694_1696delinsTAGCTT	NP_001365399.1:p.Thr565_Val566delinsIleAl...
NM_001378471.1:c.1685_1687delinsTAGCTT	NP_001365400.1:p.Thr562_Val563delinsIleAl...
NM_001378472.1:c.1640_1642delinsTAGCTT	NP_001365401.1:p.Thr547_Val548delinsIleAl...
NM_001378473.1:c.1640_1642delinsTAGCTT	NP_001365402.1:p.Thr547_Val548delinsIleAl...
NM_001378474.1:c.1796_1798delinsTAGCTT	NP_001365403.1:p.Thr599_Val600delinsIleAl...
NM_001378475.1:c.1532_1534delinsTAGCTT	NP_001365404.1:p.Thr511_Val512delinsIleAl...