Canonical Allele Identifier: CA645544105

Gene: BRAF

Linked Data

• dbSNP Id: rs2128998321
• COSMIC: COSM144982

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753338_140753340dup , CM000669.2:g.140753338_140753340dup	GRCh38
NC_000007.13:g.140453138_140453140dup , CM000669.1:g.140453138_140453140dup	GRCh37
NC_000007.12:g.140099607_140099609dup	NCBI36
NG_007873.3:g.176425_176427dup , LRG_299:g.176425_176427dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1795_1797dup MANE Select	ENSP00000493543.1:p.Thr599_Val600insThr
ENST00000288602.11:c.1915_1917dup	ENSP00000288602.7:p.Thr639_Val640insThr
ENST00000479537.6:c.465_467dup
ENST00000496384.7:c.1795_1797dup	ENSP00000419060.2:p.Thr599_Val600insThr
ENST00000497784.2:c.*1245_*1247dup	ENSP00000420119.2:n.*1245_*1247dup
ENST00000642228.1:c.*873_*875dup	ENSP00000493678.1:n.*873_*875dup
ENST00000642875.1:n.1259-3922_1259-3920dup
ENST00000644120.1:n.2185_2187dup
ENST00000644650.1:c.891_893dup
ENST00000644905.1:n.2677_2679dup
ENST00000644969.2:c.1915_1917dup MANE Plus Clinical	ENSP00000496776.1:p.Thr639_Val640insThr
ENST00000646730.1:c.*371_*373dup	ENSP00000494784.1:n.*371_*373dup
ENST00000646891.1:c.1795_1797dup	ENSP00000493543.1:p.Thr599_Val600insThr
ENST00000647434.1:c.738-3922_738-3920dup	ENSP00000495132.1:n.738-3922_738-3920dup
ENST00000288602.10:c.1795_1797dup	ENSP00000288602.6:p.Thr599_Val600insThr
ENST00000479537.5:c.79_81dup	ENSP00000418033.1:p.Thr27_Val28insThr
ENST00000496384.6:c.618_620dup
ENST00000497784.1:c.1830_1832dup	ENSP00000420119.1:n.1830_1832dup
NM_004333.4:c.1795_1797dup , LRG_299t1:c.1795_1797dup	NP_004324.2:p.Thr599_Val600insThr
XM_005250045.1:c.1795_1797dup	XP_005250102.1:p.Thr599_Val600insThr
XM_005250046.1:c.1795_1797dup	XP_005250103.1:p.Thr599_Val600insThr
XM_011516529.1:c.1795_1797dup	XP_011514831.1:p.Thr599_Val600insThr
XM_011516530.1:c.1695-3922_1695-3920dup	XP_011514832.1:n.1695-3922_1695-3920dup
XR_242190.1:n.1803_1805dup
XR_927520.1:n.1803_1805dup
XR_927521.1:n.1803_1805dup
XR_927522.1:n.1703-3922_1703-3920dup
XR_927523.1:n.1703-3922_1703-3920dup
NM_001354609.1:c.1795_1797dup	NP_001341538.1:p.Thr599_Val600insThr
NM_004333.5:c.1795_1797dup	NP_004324.2:p.Thr599_Val600insThr
NR_148928.1:n.2893_2895dup
XM_017012558.1:c.1915_1917dup	XP_016868047.1:p.Thr639_Val640insThr
XM_017012559.1:c.1915_1917dup	XP_016868048.1:p.Thr639_Val640insThr
XR_001744857.1:n.1923_1925dup
XR_001744858.1:n.1823-3922_1823-3920dup
NM_001354609.2:c.1795_1797dup	NP_001341538.1:p.Thr599_Val600insThr
NM_001374244.1:c.1915_1917dup	NP_001361173.1:p.Thr639_Val640insThr
NM_001374258.1:c.1915_1917dup MANE Plus Clinical	NP_001361187.1:p.Thr639_Val640insThr
NM_004333.6:c.1795_1797dup MANE Select	NP_004324.2:p.Thr599_Val600insThr
NM_001378467.1:c.1804_1806dup	NP_001365396.1:p.Thr602_Val603insThr
NM_001378468.1:c.1795_1797dup	NP_001365397.1:p.Thr599_Val600insThr
NM_001378469.1:c.1729_1731dup	NP_001365398.1:p.Thr577_Val578insThr
NM_001378470.1:c.1693_1695dup	NP_001365399.1:p.Thr565_Val566insThr
NM_001378471.1:c.1684_1686dup	NP_001365400.1:p.Thr562_Val563insThr
NM_001378472.1:c.1639_1641dup	NP_001365401.1:p.Thr547_Val548insThr
NM_001378473.1:c.1639_1641dup	NP_001365402.1:p.Thr547_Val548insThr
NM_001378474.1:c.1795_1797dup	NP_001365403.1:p.Thr599_Val600insThr
NM_001378475.1:c.1531_1533dup	NP_001365404.1:p.Thr511_Val512insThr