Canonical Allele Identifier: CA1747732078

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140800416_140800419delinsTCTG , CM000669.2:g.140800416_140800419delinsTCTG	GRCh38
NC_000007.13:g.140500216_140500219delinsTCTG , CM000669.1:g.140500216_140500219delinsTCTG	GRCh37
NC_000007.12:g.140146685_140146688delinsTCTG	NCBI36
NG_007873.3:g.129346_129349delinsCAGA , LRG_299:g.129346_129349delinsCAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.923_926delinsCAGA MANE Select	ENSP00000493543.1:p.Ala308=
ENST00000288602.11:c.923_926delinsCAGA	ENSP00000288602.7:p.Ala308=
ENST00000496384.7:c.923_926delinsCAGA	ENSP00000419060.2:p.Ala308=
ENST00000497784.2:c.*373_*376delinsCAGA	ENSP00000420119.2:n.*373_*376delinsCAGA
ENST00000642228.1:c.*1_*4delinsCAGA	ENSP00000493678.1:n.*1_*4delinsCAGA
ENST00000642272.1:n.955_958delinsCAGA
ENST00000642875.1:n.417_420delinsCAGA
ENST00000644120.1:n.1365_1368delinsCAGA
ENST00000644650.1:c.19_22delinsCAGA
ENST00000644905.1:n.1012_1015delinsCAGA
ENST00000644969.2:c.923_926delinsCAGA MANE Plus Clinical	ENSP00000496776.1:p.Ala308=
ENST00000646730.1:c.923_926delinsCAGA	ENSP00000494784.1:p.Ala308=
ENST00000646891.1:c.923_926delinsCAGA	ENSP00000493543.1:p.Ala308=
ENST00000288602.10:c.923_926delinsCAGA	ENSP00000288602.6:p.Ala308=
ENST00000497784.1:c.958_961delinsCAGA	ENSP00000420119.1:n.958_961delinsCAGA
NM_004333.4:c.923_926delinsCAGA , LRG_299t1:c.923_926delinsCAGA	NP_004324.2:p.Ala308=
XM_005250045.1:c.923_926delinsCAGA	XP_005250102.1:p.Ala308=
XM_005250046.1:c.923_926delinsCAGA	XP_005250103.1:p.Ala308=
XM_011516529.1:c.923_926delinsCAGA	XP_011514831.1:p.Ala308=
XM_011516530.1:c.923_926delinsCAGA	XP_011514832.1:p.Ala308=
XR_242190.1:n.931_934delinsCAGA
XR_927520.1:n.931_934delinsCAGA
XR_927521.1:n.931_934delinsCAGA
XR_927522.1:n.931_934delinsCAGA
XR_927523.1:n.931_934delinsCAGA
NM_001354609.1:c.923_926delinsCAGA	NP_001341538.1:p.Ala308=
NM_004333.5:c.923_926delinsCAGA	NP_004324.2:p.Ala308=
NR_148928.1:n.1228_1231delinsCAGA
XM_017012558.1:c.923_926delinsCAGA	XP_016868047.1:p.Ala308=
XM_017012559.1:c.923_926delinsCAGA	XP_016868048.1:p.Ala308=
XR_001744857.1:n.931_934delinsCAGA
XR_001744858.1:n.931_934delinsCAGA
NM_001354609.2:c.923_926delinsCAGA	NP_001341538.1:p.Ala308=
NM_001374244.1:c.923_926delinsCAGA	NP_001361173.1:p.Ala308=
NM_001374258.1:c.923_926delinsCAGA MANE Plus Clinical	NP_001361187.1:p.Ala308=
NM_004333.6:c.923_926delinsCAGA MANE Select	NP_004324.2:p.Ala308=
NM_001378467.1:c.932_935delinsCAGA	NP_001365396.1:p.Ala311=
NM_001378468.1:c.923_926delinsCAGA	NP_001365397.1:p.Ala308=
NM_001378469.1:c.923_926delinsCAGA	NP_001365398.1:p.Ala308=
NM_001378470.1:c.821_824delinsCAGA	NP_001365399.1:p.Ala274=
NM_001378471.1:c.923_926delinsCAGA	NP_001365400.1:p.Ala308=
NM_001378472.1:c.767_770delinsCAGA	NP_001365401.1:p.Ala256=
NM_001378473.1:c.767_770delinsCAGA	NP_001365402.1:p.Ala256=
NM_001378474.1:c.923_926delinsCAGA	NP_001365403.1:p.Ala308=
NM_001378475.1:c.659_662delinsCAGA	NP_001365404.1:p.Ala220=