Canonical Allele Identifier: CA2685244231

Gene: BRAF

Linked Data

• gnomAD v4: 7-140801032-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140801032_140801033insC , CM000669.2:g.140801032_140801033insC	GRCh38
NC_000007.13:g.140500832_140500833insC , CM000669.1:g.140500832_140500833insC	GRCh37
NC_000007.12:g.140147301_140147302insC	NCBI36
NG_007873.3:g.128732_128733insG , LRG_299:g.128732_128733insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.860+379_860+380insG MANE Select	ENSP00000493543.1:n.860+379_860+380insG
ENST00000288602.11:c.860+379_860+380insG	ENSP00000288602.7:n.860+379_860+380insG
ENST00000496384.7:c.860+379_860+380insG	ENSP00000419060.2:n.860+379_860+380insG
ENST00000497784.2:c.*310+379_*310+380insG	ENSP00000420119.2:n.*310+379_*310+380insG
ENST00000642228.1:c.860+379_860+380insG	ENSP00000493678.1:n.860+379_860+380insG
ENST00000642272.1:n.892+379_892+380insG
ENST00000642875.1:n.354+379_354+380insG
ENST00000643356.1:n.840_841insG
ENST00000644120.1:n.1302+379_1302+380insG
ENST00000644905.1:n.949+379_949+380insG
ENST00000644969.2:c.860+379_860+380insG MANE Plus Clinical	ENSP00000496776.1:n.860+379_860+380insG
ENST00000646730.1:c.860+379_860+380insG	ENSP00000494784.1:n.860+379_860+380insG
ENST00000646891.1:c.860+379_860+380insG	ENSP00000493543.1:n.860+379_860+380insG
ENST00000288602.10:c.860+379_860+380insG	ENSP00000288602.6:n.860+379_860+380insG
ENST00000497784.1:c.895+379_895+380insG	ENSP00000420119.1:n.895+379_895+380insG
NM_004333.4:c.860+379_860+380insG , LRG_299t1:c.860+379_860+380insG	NP_004324.2:n.860+379_860+380insG
XM_005250045.1:c.860+379_860+380insG	XP_005250102.1:n.860+379_860+380insG
XM_005250046.1:c.860+379_860+380insG	XP_005250103.1:n.860+379_860+380insG
XM_011516529.1:c.860+379_860+380insG	XP_011514831.1:n.860+379_860+380insG
XM_011516530.1:c.860+379_860+380insG	XP_011514832.1:n.860+379_860+380insG
XR_242190.1:n.868+379_868+380insG
XR_927520.1:n.868+379_868+380insG
XR_927521.1:n.868+379_868+380insG
XR_927522.1:n.868+379_868+380insG
XR_927523.1:n.868+379_868+380insG
NM_001354609.1:c.860+379_860+380insG	NP_001341538.1:n.860+379_860+380insG
NM_004333.5:c.860+379_860+380insG	NP_004324.2:n.860+379_860+380insG
NR_148928.1:n.1165+379_1165+380insG
XM_017012558.1:c.860+379_860+380insG	XP_016868047.1:n.860+379_860+380insG
XM_017012559.1:c.860+379_860+380insG	XP_016868048.1:n.860+379_860+380insG
XR_001744857.1:n.868+379_868+380insG
XR_001744858.1:n.868+379_868+380insG
NM_001354609.2:c.860+379_860+380insG	NP_001341538.1:n.860+379_860+380insG
NM_001374244.1:c.860+379_860+380insG	NP_001361173.1:n.860+379_860+380insG
NM_001374258.1:c.860+379_860+380insG MANE Plus Clinical	NP_001361187.1:n.860+379_860+380insG
NM_004333.6:c.860+379_860+380insG MANE Select	NP_004324.2:n.860+379_860+380insG
NM_001378467.1:c.869+379_869+380insG	NP_001365396.1:n.869+379_869+380insG
NM_001378468.1:c.860+379_860+380insG	NP_001365397.1:n.860+379_860+380insG
NM_001378469.1:c.860+379_860+380insG	NP_001365398.1:n.860+379_860+380insG
NM_001378470.1:c.758+379_758+380insG	NP_001365399.1:n.758+379_758+380insG
NM_001378471.1:c.860+379_860+380insG	NP_001365400.1:n.860+379_860+380insG
NM_001378472.1:c.704+379_704+380insG	NP_001365401.1:n.704+379_704+380insG
NM_001378473.1:c.704+379_704+380insG	NP_001365402.1:n.704+379_704+380insG
NM_001378474.1:c.860+379_860+380insG	NP_001365403.1:n.860+379_860+380insG
NM_001378475.1:c.596+379_596+380insG	NP_001365404.1:n.596+379_596+380insG