Canonical Allele Identifier: CA645544096

Gene: BRAF

Linked Data

• COSMIC: COSM5985086

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753336_140753337delinsGT , CM000669.2:g.140753336_140753337delinsGT	GRCh38
NC_000007.13:g.140453136_140453137delinsGT , CM000669.1:g.140453136_140453137delinsGT	GRCh37
NC_000007.12:g.140099605_140099606delinsGT	NCBI36
NG_007873.3:g.176428_176429delinsAC , LRG_299:g.176428_176429delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1798_1799delinsAC MANE Select	ENSP00000493543.1:p.Val600Thr
ENST00000288602.11:c.1918_1919delinsAC	ENSP00000288602.7:p.Val640Thr
ENST00000479537.6:c.468_469delinsAC
ENST00000496384.7:c.1798_1799delinsAC	ENSP00000419060.2:p.Val600Thr
ENST00000497784.2:c.*1248_*1249delinsAC	ENSP00000420119.2:n.*1248_*1249delinsAC
ENST00000642228.1:c.*876_*877delinsAC	ENSP00000493678.1:n.*876_*877delinsAC
ENST00000642875.1:n.1259-3919_1259-3918delinsAC
ENST00000644120.1:n.2188_2189delinsAC
ENST00000644650.1:c.894_895delinsAC
ENST00000644905.1:n.2680_2681delinsAC
ENST00000644969.2:c.1918_1919delinsAC MANE Plus Clinical	ENSP00000496776.1:p.Val640Thr
ENST00000646730.1:c.*374_*375delinsAC	ENSP00000494784.1:n.*374_*375delinsAC
ENST00000646891.1:c.1798_1799delinsAC	ENSP00000493543.1:p.Val600Thr
ENST00000647434.1:c.738-3919_738-3918delinsAC	ENSP00000495132.1:n.738-3919_738-3918deli...
ENST00000288602.10:c.1798_1799delinsAC	ENSP00000288602.6:p.Val600Thr
ENST00000479537.5:c.82_83delinsAC	ENSP00000418033.1:p.Val28Thr
ENST00000496384.6:c.621_622delinsAC
ENST00000497784.1:c.1833_1834delinsAC	ENSP00000420119.1:n.1833_1834delinsAC
NM_004333.4:c.1798_1799delinsAC , LRG_299t1:c.1798_1799delinsAC	NP_004324.2:p.Val600Thr
XM_005250045.1:c.1798_1799delinsAC	XP_005250102.1:p.Val600Thr
XM_005250046.1:c.1798_1799delinsAC	XP_005250103.1:p.Val600Thr
XM_011516529.1:c.1798_1799delinsAC	XP_011514831.1:p.Val600Thr
XM_011516530.1:c.1695-3919_1695-3918delinsAC	XP_011514832.1:n.1695-3919_1695-3918delin...
XR_242190.1:n.1806_1807delinsAC
XR_927520.1:n.1806_1807delinsAC
XR_927521.1:n.1806_1807delinsAC
XR_927522.1:n.1703-3919_1703-3918delinsAC
XR_927523.1:n.1703-3919_1703-3918delinsAC
NM_001354609.1:c.1798_1799delinsAC	NP_001341538.1:p.Val600Thr
NM_004333.5:c.1798_1799delinsAC	NP_004324.2:p.Val600Thr
NR_148928.1:n.2896_2897delinsAC
XM_017012558.1:c.1918_1919delinsAC	XP_016868047.1:p.Val640Thr
XM_017012559.1:c.1918_1919delinsAC	XP_016868048.1:p.Val640Thr
XR_001744857.1:n.1926_1927delinsAC
XR_001744858.1:n.1823-3919_1823-3918delinsAC
NM_001354609.2:c.1798_1799delinsAC	NP_001341538.1:p.Val600Thr
NM_001374244.1:c.1918_1919delinsAC	NP_001361173.1:p.Val640Thr
NM_001374258.1:c.1918_1919delinsAC MANE Plus Clinical	NP_001361187.1:p.Val640Thr
NM_004333.6:c.1798_1799delinsAC MANE Select	NP_004324.2:p.Val600Thr
NM_001378467.1:c.1807_1808delinsAC	NP_001365396.1:p.Val603Thr
NM_001378468.1:c.1798_1799delinsAC	NP_001365397.1:p.Val600Thr
NM_001378469.1:c.1732_1733delinsAC	NP_001365398.1:p.Val578Thr
NM_001378470.1:c.1696_1697delinsAC	NP_001365399.1:p.Val566Thr
NM_001378471.1:c.1687_1688delinsAC	NP_001365400.1:p.Val563Thr
NM_001378472.1:c.1642_1643delinsAC	NP_001365401.1:p.Val548Thr
NM_001378473.1:c.1642_1643delinsAC	NP_001365402.1:p.Val548Thr
NM_001378474.1:c.1798_1799delinsAC	NP_001365403.1:p.Val600Thr
NM_001378475.1:c.1534_1535delinsAC	NP_001365404.1:p.Val512Thr