Canonical Allele Identifier: CA2579043805

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140800550_140800551del , CM000669.2:g.140800550_140800551del	GRCh38
NC_000007.13:g.140500350_140500351del , CM000669.1:g.140500350_140500351del	GRCh37
NC_000007.12:g.140146819_140146820del	NCBI36
NG_007873.3:g.129214_129215del , LRG_299:g.129214_129215del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.861-70_861-69del MANE Select	ENSP00000493543.1:n.861-70_861-69del
ENST00000288602.11:c.861-70_861-69del	ENSP00000288602.7:n.861-70_861-69del
ENST00000496384.7:c.861-70_861-69del	ENSP00000419060.2:n.861-70_861-69del
ENST00000497784.2:c.*311-70_*311-69del	ENSP00000420119.2:n.*311-70_*311-69del
ENST00000642228.1:c.861-89_861-88del	ENSP00000493678.1:n.861-89_861-88del
ENST00000642272.1:n.893-70_893-69del
ENST00000642875.1:n.355-70_355-69del
ENST00000644120.1:n.1303-70_1303-69del
ENST00000644905.1:n.950-70_950-69del
ENST00000644969.2:c.861-70_861-69del MANE Plus Clinical	ENSP00000496776.1:n.861-70_861-69del
ENST00000646730.1:c.861-70_861-69del	ENSP00000494784.1:n.861-70_861-69del
ENST00000646891.1:c.861-70_861-69del	ENSP00000493543.1:n.861-70_861-69del
ENST00000288602.10:c.861-70_861-69del	ENSP00000288602.6:n.861-70_861-69del
ENST00000497784.1:c.896-70_896-69del	ENSP00000420119.1:n.896-70_896-69del
NM_004333.4:c.861-70_861-69del , LRG_299t1:c.861-70_861-69del	NP_004324.2:n.861-70_861-69del
XM_005250045.1:c.861-70_861-69del	XP_005250102.1:n.861-70_861-69del
XM_005250046.1:c.861-70_861-69del	XP_005250103.1:n.861-70_861-69del
XM_011516529.1:c.861-70_861-69del	XP_011514831.1:n.861-70_861-69del
XM_011516530.1:c.861-70_861-69del	XP_011514832.1:n.861-70_861-69del
XR_242190.1:n.869-70_869-69del
XR_927520.1:n.869-70_869-69del
XR_927521.1:n.869-70_869-69del
XR_927522.1:n.869-70_869-69del
XR_927523.1:n.869-70_869-69del
NM_001354609.1:c.861-70_861-69del	NP_001341538.1:n.861-70_861-69del
NM_004333.5:c.861-70_861-69del	NP_004324.2:n.861-70_861-69del
NR_148928.1:n.1166-70_1166-69del
XM_017012558.1:c.861-70_861-69del	XP_016868047.1:n.861-70_861-69del
XM_017012559.1:c.861-70_861-69del	XP_016868048.1:n.861-70_861-69del
XR_001744857.1:n.869-70_869-69del
XR_001744858.1:n.869-70_869-69del
NM_001354609.2:c.861-70_861-69del	NP_001341538.1:n.861-70_861-69del
NM_001374244.1:c.861-70_861-69del	NP_001361173.1:n.861-70_861-69del
NM_001374258.1:c.861-70_861-69del MANE Plus Clinical	NP_001361187.1:n.861-70_861-69del
NM_004333.6:c.861-70_861-69del MANE Select	NP_004324.2:n.861-70_861-69del
NM_001378467.1:c.870-70_870-69del	NP_001365396.1:n.870-70_870-69del
NM_001378468.1:c.861-70_861-69del	NP_001365397.1:n.861-70_861-69del
NM_001378469.1:c.861-70_861-69del	NP_001365398.1:n.861-70_861-69del
NM_001378470.1:c.759-70_759-69del	NP_001365399.1:n.759-70_759-69del
NM_001378471.1:c.861-70_861-69del	NP_001365400.1:n.861-70_861-69del
NM_001378472.1:c.705-70_705-69del	NP_001365401.1:n.705-70_705-69del
NM_001378473.1:c.705-70_705-69del	NP_001365402.1:n.705-70_705-69del
NM_001378474.1:c.861-70_861-69del	NP_001365403.1:n.861-70_861-69del
NM_001378475.1:c.597-70_597-69del	NP_001365404.1:n.597-70_597-69del