Canonical Allele Identifier: CA645544092

Gene: BRAF

Linked Data

• COSMIC: COSM5982023
• CIViC: CA645544092

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753332_140753336delinsAT , CM000669.2:g.140753332_140753336delinsAT	GRCh38
NC_000007.13:g.140453132_140453136delinsAT , CM000669.1:g.140453132_140453136delinsAT	GRCh37
NC_000007.12:g.140099601_140099605delinsAT	NCBI36
NG_007873.3:g.176429_176433delinsAT , LRG_299:g.176429_176433delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1799_1803delinsAT MANE Select	ENSP00000493543.1:p.Val600_Lys601delinsAs...
ENST00000288602.11:c.1919_1923delinsAT	ENSP00000288602.7:p.Val640_Lys641delinsAs...
ENST00000479537.6:c.469_473delinsAT
ENST00000496384.7:c.1799_1803delinsAT	ENSP00000419060.2:p.Val600_Lys601delinsAs...
ENST00000497784.2:c.*1249_*1253delinsAT	ENSP00000420119.2:n.*1249_*1253delinsAT
ENST00000642228.1:c.*877_*881delinsAT	ENSP00000493678.1:n.*877_*881delinsAT
ENST00000642875.1:n.1259-3918_1259-3914delinsAT
ENST00000644120.1:n.2189_2193delinsAT
ENST00000644650.1:c.895_899delinsAT
ENST00000644905.1:n.2681_2685delinsAT
ENST00000644969.2:c.1919_1923delinsAT MANE Plus Clinical	ENSP00000496776.1:p.Val640_Lys641delinsAs...
ENST00000646730.1:c.*375_*379delinsAT	ENSP00000494784.1:n.*375_*379delinsAT
ENST00000646891.1:c.1799_1803delinsAT	ENSP00000493543.1:p.Val600_Lys601delinsAs...
ENST00000647434.1:c.738-3918_738-3914delinsAT	ENSP00000495132.1:n.738-3918_738-3914deli...
ENST00000288602.10:c.1799_1803delinsAT	ENSP00000288602.6:p.Val600_Lys601delinsAs...
ENST00000479537.5:c.83_87delinsAT	ENSP00000418033.1:p.Val28_Lys29delinsAsp
ENST00000496384.6:c.622_626delinsAT
ENST00000497784.1:c.1834_1838delinsAT	ENSP00000420119.1:n.1834_1838delinsAT
NM_004333.4:c.1799_1803delinsAT , LRG_299t1:c.1799_1803delinsAT	NP_004324.2:p.Val600_Lys601delinsAsp
XM_005250045.1:c.1799_1803delinsAT	XP_005250102.1:p.Val600_Lys601delinsAsp
XM_005250046.1:c.1799_1803delinsAT	XP_005250103.1:p.Val600_Lys601delinsAsp
XM_011516529.1:c.1799_1803delinsAT	XP_011514831.1:p.Val600_Lys601delinsAsp
XM_011516530.1:c.1695-3918_1695-3914delinsAT	XP_011514832.1:n.1695-3918_1695-3914delin...
XR_242190.1:n.1807_1811delinsAT
XR_927520.1:n.1807_1811delinsAT
XR_927521.1:n.1807_1811delinsAT
XR_927522.1:n.1703-3918_1703-3914delinsAT
XR_927523.1:n.1703-3918_1703-3914delinsAT
NM_001354609.1:c.1799_1803delinsAT	NP_001341538.1:p.Val600_Lys601delinsAsp
NM_004333.5:c.1799_1803delinsAT	NP_004324.2:p.Val600_Lys601delinsAsp
NR_148928.1:n.2897_2901delinsAT
XM_017012558.1:c.1919_1923delinsAT	XP_016868047.1:p.Val640_Lys641delinsAsp
XM_017012559.1:c.1919_1923delinsAT	XP_016868048.1:p.Val640_Lys641delinsAsp
XR_001744857.1:n.1927_1931delinsAT
XR_001744858.1:n.1823-3918_1823-3914delinsAT
NM_001354609.2:c.1799_1803delinsAT	NP_001341538.1:p.Val600_Lys601delinsAsp
NM_001374244.1:c.1919_1923delinsAT	NP_001361173.1:p.Val640_Lys641delinsAsp
NM_001374258.1:c.1919_1923delinsAT MANE Plus Clinical	NP_001361187.1:p.Val640_Lys641delinsAsp
NM_004333.6:c.1799_1803delinsAT MANE Select	NP_004324.2:p.Val600_Lys601delinsAsp
NM_001378467.1:c.1808_1812delinsAT	NP_001365396.1:p.Val603_Lys604delinsAsp
NM_001378468.1:c.1799_1803delinsAT	NP_001365397.1:p.Val600_Lys601delinsAsp
NM_001378469.1:c.1733_1737delinsAT	NP_001365398.1:p.Val578_Lys579delinsAsp
NM_001378470.1:c.1697_1701delinsAT	NP_001365399.1:p.Val566_Lys567delinsAsp
NM_001378471.1:c.1688_1692delinsAT	NP_001365400.1:p.Val563_Lys564delinsAsp
NM_001378472.1:c.1643_1647delinsAT	NP_001365401.1:p.Val548_Lys549delinsAsp
NM_001378473.1:c.1643_1647delinsAT	NP_001365402.1:p.Val548_Lys549delinsAsp
NM_001378474.1:c.1799_1803delinsAT	NP_001365403.1:p.Val600_Lys601delinsAsp
NM_001378475.1:c.1535_1539delinsAT	NP_001365404.1:p.Val512_Lys513delinsAsp