Canonical Allele Identifier: CA645544089

Gene: BRAF

Linked Data

• COSMIC: COSM30605

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753326_140753339delinsGA , CM000669.2:g.140753326_140753339delinsGA	GRCh38
NC_000007.13:g.140453126_140453139delinsGA , CM000669.1:g.140453126_140453139delinsGA	GRCh37
NC_000007.12:g.140099595_140099608delinsGA	NCBI36
NG_007873.3:g.176426_176439delinsTC , LRG_299:g.176426_176439delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1796_1809delinsTC MANE Select	ENSP00000493543.1:p.Thr599_Arg603delinsIl...
ENST00000288602.11:c.1916_1929delinsTC	ENSP00000288602.7:p.Thr639_Arg643delinsIl...
ENST00000479537.6:c.466_479delinsTC
ENST00000496384.7:c.1796_1809delinsTC	ENSP00000419060.2:p.Thr599_Arg603delinsIl...
ENST00000497784.2:c.*1246_*1259delinsTC	ENSP00000420119.2:n.*1246_*1259delinsTC
ENST00000642228.1:c.*874_*887delinsTC	ENSP00000493678.1:n.*874_*887delinsTC
ENST00000642875.1:n.1259-3921_1259-3908delinsTC
ENST00000644120.1:n.2186_2199delinsTC
ENST00000644650.1:c.892_905delinsTC
ENST00000644905.1:n.2678_2691delinsTC
ENST00000644969.2:c.1916_1929delinsTC MANE Plus Clinical	ENSP00000496776.1:p.Thr639_Arg643delinsIl...
ENST00000646730.1:c.*372_*385delinsTC	ENSP00000494784.1:n.*372_*385delinsTC
ENST00000646891.1:c.1796_1809delinsTC	ENSP00000493543.1:p.Thr599_Arg603delinsIl...
ENST00000647434.1:c.738-3921_738-3908delinsTC	ENSP00000495132.1:n.738-3921_738-3908deli...
ENST00000288602.10:c.1796_1809delinsTC	ENSP00000288602.6:p.Thr599_Arg603delinsIl...
ENST00000479537.5:c.80_93delinsTC	ENSP00000418033.1:p.Thr27_Arg31delinsIle
ENST00000496384.6:c.619_632delinsTC
ENST00000497784.1:c.1831_1844delinsTC	ENSP00000420119.1:n.1831_1844delinsTC
NM_004333.4:c.1796_1809delinsTC , LRG_299t1:c.1796_1809delinsTC	NP_004324.2:p.Thr599_Arg603delinsIle
XM_005250045.1:c.1796_1809delinsTC	XP_005250102.1:p.Thr599_Arg603delinsIle
XM_005250046.1:c.1796_1809delinsTC	XP_005250103.1:p.Thr599_Arg603delinsIle
XM_011516529.1:c.1796_1809delinsTC	XP_011514831.1:p.Thr599_Arg603delinsIle
XM_011516530.1:c.1695-3921_1695-3908delinsTC	XP_011514832.1:n.1695-3921_1695-3908delin...
XR_242190.1:n.1804_1817delinsTC
XR_927520.1:n.1804_1817delinsTC
XR_927521.1:n.1804_1817delinsTC
XR_927522.1:n.1703-3921_1703-3908delinsTC
XR_927523.1:n.1703-3921_1703-3908delinsTC
NM_001354609.1:c.1796_1809delinsTC	NP_001341538.1:p.Thr599_Arg603delinsIle
NM_004333.5:c.1796_1809delinsTC	NP_004324.2:p.Thr599_Arg603delinsIle
NR_148928.1:n.2894_2907delinsTC
XM_017012558.1:c.1916_1929delinsTC	XP_016868047.1:p.Thr639_Arg643delinsIle
XM_017012559.1:c.1916_1929delinsTC	XP_016868048.1:p.Thr639_Arg643delinsIle
XR_001744857.1:n.1924_1937delinsTC
XR_001744858.1:n.1823-3921_1823-3908delinsTC
NM_001354609.2:c.1796_1809delinsTC	NP_001341538.1:p.Thr599_Arg603delinsIle
NM_001374244.1:c.1916_1929delinsTC	NP_001361173.1:p.Thr639_Arg643delinsIle
NM_001374258.1:c.1916_1929delinsTC MANE Plus Clinical	NP_001361187.1:p.Thr639_Arg643delinsIle
NM_004333.6:c.1796_1809delinsTC MANE Select	NP_004324.2:p.Thr599_Arg603delinsIle
NM_001378467.1:c.1805_1818delinsTC	NP_001365396.1:p.Thr602_Arg606delinsIle
NM_001378468.1:c.1796_1809delinsTC	NP_001365397.1:p.Thr599_Arg603delinsIle
NM_001378469.1:c.1730_1743delinsTC	NP_001365398.1:p.Thr577_Arg581delinsIle
NM_001378470.1:c.1694_1707delinsTC	NP_001365399.1:p.Thr565_Arg569delinsIle
NM_001378471.1:c.1685_1698delinsTC	NP_001365400.1:p.Thr562_Arg566delinsIle
NM_001378472.1:c.1640_1653delinsTC	NP_001365401.1:p.Thr547_Arg551delinsIle
NM_001378473.1:c.1640_1653delinsTC	NP_001365402.1:p.Thr547_Arg551delinsIle
NM_001378474.1:c.1796_1809delinsTC	NP_001365403.1:p.Thr599_Arg603delinsIle
NM_001378475.1:c.1532_1545delinsTC	NP_001365404.1:p.Thr511_Arg515delinsIle