Canonical Allele Identifier: CA1107947471

Gene: BRAF

Linked Data

• dbSNP Id: rs1800849261
• gnomAD v3: 7-140781296-C-CTT
• gnomAD v4: 7-140781296-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140781297_140781298insTT , CM000669.2:g.140781297_140781298insTT	GRCh38
NC_000007.13:g.140481097_140481098insTT , CM000669.1:g.140481097_140481098insTT	GRCh37
NC_000007.12:g.140127566_140127567insTT	NCBI36
NG_007873.3:g.148468_148469insAA , LRG_299:g.148468_148469insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1432+279_1432+280insAA MANE Select	ENSP00000493543.1:n.1432+279_1432+280insAA
ENST00000288602.11:c.1552+279_1552+280insAA	ENSP00000288602.7:n.1552+279_1552+280insAA
ENST00000479537.6:c.102+279_102+280insAA
ENST00000496384.7:c.1432+279_1432+280insAA	ENSP00000419060.2:n.1432+279_1432+280insAA
ENST00000497784.2:c.*882+279_*882+280insAA	ENSP00000420119.2:n.*882+279_*882+280insAA
ENST00000642228.1:c.*510+279_*510+280insAA	ENSP00000493678.1:n.*510+279_*510+280insAA
ENST00000642875.1:n.874+279_874+280insAA
ENST00000644120.1:n.1822+279_1822+280insAA
ENST00000644650.1:c.528+279_528+280insAA
ENST00000644905.1:n.1521+279_1521+280insAA
ENST00000644969.2:c.1552+279_1552+280insAA MANE Plus Clinical	ENSP00000496776.1:n.1552+279_1552+280insAA
ENST00000646334.1:n.841_842insAA
ENST00000646730.1:c.1432+279_1432+280insAA	ENSP00000494784.1:n.1432+279_1432+280insAA
ENST00000646891.1:c.1432+279_1432+280insAA	ENSP00000493543.1:n.1432+279_1432+280insAA
ENST00000647434.1:c.475+279_475+280insAA	ENSP00000495132.1:n.475+279_475+280insAA
ENST00000288602.10:c.1432+279_1432+280insAA	ENSP00000288602.6:n.1432+279_1432+280insAA
ENST00000496384.6:c.255+279_255+280insAA
ENST00000497784.1:c.1467+279_1467+280insAA	ENSP00000420119.1:n.1467+279_1467+280insAA
NM_004333.4:c.1432+279_1432+280insAA , LRG_299t1:c.1432+279_1432+280insAA	NP_004324.2:n.1432+279_1432+280insAA
XM_005250045.1:c.1432+279_1432+280insAA	XP_005250102.1:n.1432+279_1432+280insAA
XM_005250046.1:c.1432+279_1432+280insAA	XP_005250103.1:n.1432+279_1432+280insAA
XM_011516529.1:c.1432+279_1432+280insAA	XP_011514831.1:n.1432+279_1432+280insAA
XM_011516530.1:c.1432+279_1432+280insAA	XP_011514832.1:n.1432+279_1432+280insAA
XR_242190.1:n.1440+279_1440+280insAA
XR_927520.1:n.1440+279_1440+280insAA
XR_927521.1:n.1440+279_1440+280insAA
XR_927522.1:n.1440+279_1440+280insAA
XR_927523.1:n.1440+279_1440+280insAA
NM_001354609.1:c.1432+279_1432+280insAA	NP_001341538.1:n.1432+279_1432+280insAA
NM_004333.5:c.1432+279_1432+280insAA	NP_004324.2:n.1432+279_1432+280insAA
NR_148928.1:n.1737+279_1737+280insAA
XM_017012558.1:c.1552+279_1552+280insAA	XP_016868047.1:n.1552+279_1552+280insAA
XM_017012559.1:c.1552+279_1552+280insAA	XP_016868048.1:n.1552+279_1552+280insAA
XR_001744857.1:n.1560+279_1560+280insAA
XR_001744858.1:n.1560+279_1560+280insAA
NM_001354609.2:c.1432+279_1432+280insAA	NP_001341538.1:n.1432+279_1432+280insAA
NM_001374244.1:c.1552+279_1552+280insAA	NP_001361173.1:n.1552+279_1552+280insAA
NM_001374258.1:c.1552+279_1552+280insAA MANE Plus Clinical	NP_001361187.1:n.1552+279_1552+280insAA
NM_004333.6:c.1432+279_1432+280insAA MANE Select	NP_004324.2:n.1432+279_1432+280insAA
NM_001378467.1:c.1441+279_1441+280insAA	NP_001365396.1:n.1441+279_1441+280insAA
NM_001378468.1:c.1432+279_1432+280insAA	NP_001365397.1:n.1432+279_1432+280insAA
NM_001378469.1:c.1366+279_1366+280insAA	NP_001365398.1:n.1366+279_1366+280insAA
NM_001378470.1:c.1330+279_1330+280insAA	NP_001365399.1:n.1330+279_1330+280insAA
NM_001378471.1:c.1321+279_1321+280insAA	NP_001365400.1:n.1321+279_1321+280insAA
NM_001378472.1:c.1276+279_1276+280insAA	NP_001365401.1:n.1276+279_1276+280insAA
NM_001378473.1:c.1276+279_1276+280insAA	NP_001365402.1:n.1276+279_1276+280insAA
NM_001378474.1:c.1432+279_1432+280insAA	NP_001365403.1:n.1432+279_1432+280insAA
NM_001378475.1:c.1168+279_1168+280insAA	NP_001365404.1:n.1168+279_1168+280insAA