Canonical Allele Identifier: CA645544095

Gene: BRAF

Linked Data

• dbSNP Id: rs2128998296
• COSMIC: COSM1735763

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753336_140753339delinsTTTA , CM000669.2:g.140753336_140753339delinsTTTA	GRCh38
NC_000007.13:g.140453136_140453139delinsTTTA , CM000669.1:g.140453136_140453139delinsTTTA	GRCh37
NC_000007.12:g.140099605_140099608delinsTTTA	NCBI36
NG_007873.3:g.176426_176429delinsTAAA , LRG_299:g.176426_176429delinsTAAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1796_1799delinsTAAA MANE Select	ENSP00000493543.1:p.Thr599_Val600delinsIl...
ENST00000288602.11:c.1916_1919delinsTAAA	ENSP00000288602.7:p.Thr639_Val640delinsIl...
ENST00000479537.6:c.466_469delinsTAAA
ENST00000496384.7:c.1796_1799delinsTAAA	ENSP00000419060.2:p.Thr599_Val600delinsIl...
ENST00000497784.2:c.*1246_*1249delinsTAAA	ENSP00000420119.2:n.*1246_*1249delinsTAAA...
ENST00000642228.1:c.*874_*877delinsTAAA	ENSP00000493678.1:n.*874_*877delinsTAAA
ENST00000642875.1:n.1259-3921_1259-3918delinsTAAA
ENST00000644120.1:n.2186_2189delinsTAAA
ENST00000644650.1:c.892_895delinsTAAA
ENST00000644905.1:n.2678_2681delinsTAAA
ENST00000644969.2:c.1916_1919delinsTAAA MANE Plus Clinical	ENSP00000496776.1:p.Thr639_Val640delinsIl...
ENST00000646730.1:c.*372_*375delinsTAAA	ENSP00000494784.1:n.*372_*375delinsTAAA
ENST00000646891.1:c.1796_1799delinsTAAA	ENSP00000493543.1:p.Thr599_Val600delinsIl...
ENST00000647434.1:c.738-3921_738-3918delinsTAAA	ENSP00000495132.1:n.738-3921_738-3918deli...
ENST00000288602.10:c.1796_1799delinsTAAA	ENSP00000288602.6:p.Thr599_Val600delinsIl...
ENST00000479537.5:c.80_83delinsTAAA	ENSP00000418033.1:p.Thr27_Val28delinsIleL...
ENST00000496384.6:c.619_622delinsTAAA
ENST00000497784.1:c.1831_1834delinsTAAA	ENSP00000420119.1:n.1831_1834delinsTAAA
NM_004333.4:c.1796_1799delinsTAAA , LRG_299t1:c.1796_1799delinsTAAA	NP_004324.2:p.Thr599_Val600delinsIleLys
XM_005250045.1:c.1796_1799delinsTAAA	XP_005250102.1:p.Thr599_Val600delinsIleLy...
XM_005250046.1:c.1796_1799delinsTAAA	XP_005250103.1:p.Thr599_Val600delinsIleLy...
XM_011516529.1:c.1796_1799delinsTAAA	XP_011514831.1:p.Thr599_Val600delinsIleLy...
XM_011516530.1:c.1695-3921_1695-3918delinsTAAA	XP_011514832.1:n.1695-3921_1695-3918delin...
XR_242190.1:n.1804_1807delinsTAAA
XR_927520.1:n.1804_1807delinsTAAA
XR_927521.1:n.1804_1807delinsTAAA
XR_927522.1:n.1703-3921_1703-3918delinsTAAA
XR_927523.1:n.1703-3921_1703-3918delinsTAAA
NM_001354609.1:c.1796_1799delinsTAAA	NP_001341538.1:p.Thr599_Val600delinsIleLy...
NM_004333.5:c.1796_1799delinsTAAA	NP_004324.2:p.Thr599_Val600delinsIleLys
NR_148928.1:n.2894_2897delinsTAAA
XM_017012558.1:c.1916_1919delinsTAAA	XP_016868047.1:p.Thr639_Val640delinsIleLy...
XM_017012559.1:c.1916_1919delinsTAAA	XP_016868048.1:p.Thr639_Val640delinsIleLy...
XR_001744857.1:n.1924_1927delinsTAAA
XR_001744858.1:n.1823-3921_1823-3918delinsTAAA
NM_001354609.2:c.1796_1799delinsTAAA	NP_001341538.1:p.Thr599_Val600delinsIleLy...
NM_001374244.1:c.1916_1919delinsTAAA	NP_001361173.1:p.Thr639_Val640delinsIleLy...
NM_001374258.1:c.1916_1919delinsTAAA MANE Plus Clinical	NP_001361187.1:p.Thr639_Val640delinsIleLy...
NM_004333.6:c.1796_1799delinsTAAA MANE Select	NP_004324.2:p.Thr599_Val600delinsIleLys
NM_001378467.1:c.1805_1808delinsTAAA	NP_001365396.1:p.Thr602_Val603delinsIleLy...
NM_001378468.1:c.1796_1799delinsTAAA	NP_001365397.1:p.Thr599_Val600delinsIleLy...
NM_001378469.1:c.1730_1733delinsTAAA	NP_001365398.1:p.Thr577_Val578delinsIleLy...
NM_001378470.1:c.1694_1697delinsTAAA	NP_001365399.1:p.Thr565_Val566delinsIleLy...
NM_001378471.1:c.1685_1688delinsTAAA	NP_001365400.1:p.Thr562_Val563delinsIleLy...
NM_001378472.1:c.1640_1643delinsTAAA	NP_001365401.1:p.Thr547_Val548delinsIleLy...
NM_001378473.1:c.1640_1643delinsTAAA	NP_001365402.1:p.Thr547_Val548delinsIleLy...
NM_001378474.1:c.1796_1799delinsTAAA	NP_001365403.1:p.Thr599_Val600delinsIleLy...
NM_001378475.1:c.1532_1535delinsTAAA	NP_001365404.1:p.Thr511_Val512delinsIleLy...