Canonical Allele Identifier: CA1747725977

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140776973_140776976delinsCAAT , CM000669.2:g.140776973_140776976delinsCAAT	GRCh38
NC_000007.13:g.140476773_140476776delinsCAAT , CM000669.1:g.140476773_140476776delinsCAAT	GRCh37
NC_000007.12:g.140123242_140123245delinsCAAT	NCBI36
NG_007873.3:g.152789_152792delinsATTG , LRG_299:g.152789_152792delinsATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1630_1633delinsATTG MANE Select	ENSP00000493543.1:p.Ile544=
ENST00000288602.11:c.1750_1753delinsATTG	ENSP00000288602.7:p.Ile584=
ENST00000479537.6:c.300_303delinsATTG
ENST00000496384.7:c.1630_1633delinsATTG	ENSP00000419060.2:p.Ile544=
ENST00000497784.2:c.*1080_*1083delinsATTG	ENSP00000420119.2:n.*1080_*1083delinsATTG
ENST00000642228.1:c.*708_*711delinsATTG	ENSP00000493678.1:n.*708_*711delinsATTG
ENST00000642875.1:n.1194_1197delinsATTG
ENST00000644120.1:n.2020_2023delinsATTG
ENST00000644650.1:c.726_729delinsATTG
ENST00000644905.1:n.1719_1722delinsATTG
ENST00000644969.2:c.1750_1753delinsATTG MANE Plus Clinical	ENSP00000496776.1:p.Ile584=
ENST00000646730.1:c.1630_1633delinsATTG	ENSP00000494784.1:p.Ile544=
ENST00000646891.1:c.1630_1633delinsATTG	ENSP00000493543.1:p.Ile544=
ENST00000647434.1:c.673_676delinsATTG	ENSP00000495132.1:p.Ile225=
ENST00000288602.10:c.1630_1633delinsATTG	ENSP00000288602.6:p.Ile544=
ENST00000496384.6:c.453_456delinsATTG
ENST00000497784.1:c.1665_1668delinsATTG	ENSP00000420119.1:n.1665_1668delinsATTG
NM_004333.4:c.1630_1633delinsATTG , LRG_299t1:c.1630_1633delinsATTG	NP_004324.2:p.Ile544=
XM_005250045.1:c.1630_1633delinsATTG	XP_005250102.1:p.Ile544=
XM_005250046.1:c.1630_1633delinsATTG	XP_005250103.1:p.Ile544=
XM_011516529.1:c.1630_1633delinsATTG	XP_011514831.1:p.Ile544=
XM_011516530.1:c.1630_1633delinsATTG	XP_011514832.1:p.Ile544=
XR_242190.1:n.1638_1641delinsATTG
XR_927520.1:n.1638_1641delinsATTG
XR_927521.1:n.1638_1641delinsATTG
XR_927522.1:n.1638_1641delinsATTG
XR_927523.1:n.1638_1641delinsATTG
NM_001354609.1:c.1630_1633delinsATTG	NP_001341538.1:p.Ile544=
NM_004333.5:c.1630_1633delinsATTG	NP_004324.2:p.Ile544=
NR_148928.1:n.1935_1938delinsATTG
XM_017012558.1:c.1750_1753delinsATTG	XP_016868047.1:p.Ile584=
XM_017012559.1:c.1750_1753delinsATTG	XP_016868048.1:p.Ile584=
XR_001744857.1:n.1758_1761delinsATTG
XR_001744858.1:n.1758_1761delinsATTG
NM_001354609.2:c.1630_1633delinsATTG	NP_001341538.1:p.Ile544=
NM_001374244.1:c.1750_1753delinsATTG	NP_001361173.1:p.Ile584=
NM_001374258.1:c.1750_1753delinsATTG MANE Plus Clinical	NP_001361187.1:p.Ile584=
NM_004333.6:c.1630_1633delinsATTG MANE Select	NP_004324.2:p.Ile544=
NM_001378467.1:c.1639_1642delinsATTG	NP_001365396.1:p.Ile547=
NM_001378468.1:c.1630_1633delinsATTG	NP_001365397.1:p.Ile544=
NM_001378469.1:c.1564_1567delinsATTG	NP_001365398.1:p.Ile522=
NM_001378470.1:c.1528_1531delinsATTG	NP_001365399.1:p.Ile510=
NM_001378471.1:c.1519_1522delinsATTG	NP_001365400.1:p.Ile507=
NM_001378472.1:c.1474_1477delinsATTG	NP_001365401.1:p.Ile492=
NM_001378473.1:c.1474_1477delinsATTG	NP_001365402.1:p.Ile492=
NM_001378474.1:c.1630_1633delinsATTG	NP_001365403.1:p.Ile544=
NM_001378475.1:c.1366_1369delinsATTG	NP_001365404.1:p.Ile456=