Canonical Allele Identifier: CA1747710006

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753336_140753337delinsAC , CM000669.2:g.140753336_140753337delinsAC	GRCh38
NC_000007.13:g.140453136_140453137delinsAC , CM000669.1:g.140453136_140453137delinsAC	GRCh37
NC_000007.12:g.140099605_140099606delinsAC	NCBI36
NG_007873.3:g.176428_176429delinsGT , LRG_299:g.176428_176429delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1798_1799delinsGT MANE Select	ENSP00000493543.1:p.Val600=
ENST00000288602.11:c.1918_1919delinsGT	ENSP00000288602.7:p.Val640=
ENST00000479537.6:c.468_469delinsGT
ENST00000496384.7:c.1798_1799delinsGT	ENSP00000419060.2:p.Val600=
ENST00000497784.2:c.*1248_*1249delinsGT	ENSP00000420119.2:n.*1248_*1249delinsGT
ENST00000642228.1:c.*876_*877delinsGT	ENSP00000493678.1:n.*876_*877delinsGT
ENST00000642875.1:n.1259-3919_1259-3918delinsGT
ENST00000644120.1:n.2188_2189delinsGT
ENST00000644650.1:c.894_895delinsGT
ENST00000644905.1:n.2680_2681delinsGT
ENST00000644969.2:c.1918_1919delinsGT MANE Plus Clinical	ENSP00000496776.1:p.Val640=
ENST00000646730.1:c.*374_*375delinsGT	ENSP00000494784.1:n.*374_*375delinsGT
ENST00000646891.1:c.1798_1799delinsGT	ENSP00000493543.1:p.Val600=
ENST00000647434.1:c.738-3919_738-3918delinsGT	ENSP00000495132.1:n.738-3919_738-3918deli...
ENST00000288602.10:c.1798_1799delinsGT	ENSP00000288602.6:p.Val600=
ENST00000479537.5:c.82_83delinsGT	ENSP00000418033.1:p.Val28=
ENST00000496384.6:c.621_622delinsGT
ENST00000497784.1:c.1833_1834delinsGT	ENSP00000420119.1:n.1833_1834delinsGT
NM_004333.4:c.1798_1799delinsGT , LRG_299t1:c.1798_1799delinsGT	NP_004324.2:p.Val600=
XM_005250045.1:c.1798_1799delinsGT	XP_005250102.1:p.Val600=
XM_005250046.1:c.1798_1799delinsGT	XP_005250103.1:p.Val600=
XM_011516529.1:c.1798_1799delinsGT	XP_011514831.1:p.Val600=
XM_011516530.1:c.1695-3919_1695-3918delinsGT	XP_011514832.1:n.1695-3919_1695-3918delin...
XR_242190.1:n.1806_1807delinsGT
XR_927520.1:n.1806_1807delinsGT
XR_927521.1:n.1806_1807delinsGT
XR_927522.1:n.1703-3919_1703-3918delinsGT
XR_927523.1:n.1703-3919_1703-3918delinsGT
NM_001354609.1:c.1798_1799delinsGT	NP_001341538.1:p.Val600=
NM_004333.5:c.1798_1799delinsGT	NP_004324.2:p.Val600=
NR_148928.1:n.2896_2897delinsGT
XM_017012558.1:c.1918_1919delinsGT	XP_016868047.1:p.Val640=
XM_017012559.1:c.1918_1919delinsGT	XP_016868048.1:p.Val640=
XR_001744857.1:n.1926_1927delinsGT
XR_001744858.1:n.1823-3919_1823-3918delinsGT
NM_001354609.2:c.1798_1799delinsGT	NP_001341538.1:p.Val600=
NM_001374244.1:c.1918_1919delinsGT	NP_001361173.1:p.Val640=
NM_001374258.1:c.1918_1919delinsGT MANE Plus Clinical	NP_001361187.1:p.Val640=
NM_004333.6:c.1798_1799delinsGT MANE Select	NP_004324.2:p.Val600=
NM_001378467.1:c.1807_1808delinsGT	NP_001365396.1:p.Val603=
NM_001378468.1:c.1798_1799delinsGT	NP_001365397.1:p.Val600=
NM_001378469.1:c.1732_1733delinsGT	NP_001365398.1:p.Val578=
NM_001378470.1:c.1696_1697delinsGT	NP_001365399.1:p.Val566=
NM_001378471.1:c.1687_1688delinsGT	NP_001365400.1:p.Val563=
NM_001378472.1:c.1642_1643delinsGT	NP_001365401.1:p.Val548=
NM_001378473.1:c.1642_1643delinsGT	NP_001365402.1:p.Val548=
NM_001378474.1:c.1798_1799delinsGT	NP_001365403.1:p.Val600=
NM_001378475.1:c.1534_1535delinsGT	NP_001365404.1:p.Val512=