Canonical Allele Identifier: CA2685241217

Gene: BRAF

Linked Data

• gnomAD v4: 7-140778158-TATC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140778161_140778163del , CM000669.2:g.140778161_140778163del	GRCh38
NC_000007.13:g.140477961_140477963del , CM000669.1:g.140477961_140477963del	GRCh37
NC_000007.12:g.140124430_140124432del	NCBI36
NG_007873.3:g.151604_151606del , LRG_299:g.151604_151606del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1433-86_1433-84del MANE Select	ENSP00000493543.1:n.1433-86_1433-84del
ENST00000288602.11:c.1553-86_1553-84del	ENSP00000288602.7:n.1553-86_1553-84del
ENST00000479537.6:c.103-86_103-84del
ENST00000496384.7:c.1433-86_1433-84del	ENSP00000419060.2:n.1433-86_1433-84del
ENST00000497784.2:c.*883-86_*883-84del	ENSP00000420119.2:n.*883-86_*883-84del
ENST00000642228.1:c.*511-86_*511-84del	ENSP00000493678.1:n.*511-86_*511-84del
ENST00000642875.1:n.997-86_997-84del
ENST00000644120.1:n.1823-86_1823-84del
ENST00000644650.1:c.529-86_529-84del
ENST00000644905.1:n.1522-86_1522-84del
ENST00000644969.2:c.1553-86_1553-84del MANE Plus Clinical	ENSP00000496776.1:n.1553-86_1553-84del
ENST00000646730.1:c.1433-86_1433-84del	ENSP00000494784.1:n.1433-86_1433-84del
ENST00000646891.1:c.1433-86_1433-84del	ENSP00000493543.1:n.1433-86_1433-84del
ENST00000647434.1:c.476-86_476-84del	ENSP00000495132.1:n.476-86_476-84del
ENST00000288602.10:c.1433-86_1433-84del	ENSP00000288602.6:n.1433-86_1433-84del
ENST00000496384.6:c.256-86_256-84del
ENST00000497784.1:c.1468-86_1468-84del	ENSP00000420119.1:n.1468-86_1468-84del
NM_004333.4:c.1433-86_1433-84del , LRG_299t1:c.1433-86_1433-84del	NP_004324.2:n.1433-86_1433-84del
XM_005250045.1:c.1433-86_1433-84del	XP_005250102.1:n.1433-86_1433-84del
XM_005250046.1:c.1433-86_1433-84del	XP_005250103.1:n.1433-86_1433-84del
XM_011516529.1:c.1433-86_1433-84del	XP_011514831.1:n.1433-86_1433-84del
XM_011516530.1:c.1433-86_1433-84del	XP_011514832.1:n.1433-86_1433-84del
XR_242190.1:n.1441-86_1441-84del
XR_927520.1:n.1441-86_1441-84del
XR_927521.1:n.1441-86_1441-84del
XR_927522.1:n.1441-86_1441-84del
XR_927523.1:n.1441-86_1441-84del
NM_001354609.1:c.1433-86_1433-84del	NP_001341538.1:n.1433-86_1433-84del
NM_004333.5:c.1433-86_1433-84del	NP_004324.2:n.1433-86_1433-84del
NR_148928.1:n.1738-86_1738-84del
XM_017012558.1:c.1553-86_1553-84del	XP_016868047.1:n.1553-86_1553-84del
XM_017012559.1:c.1553-86_1553-84del	XP_016868048.1:n.1553-86_1553-84del
XR_001744857.1:n.1561-86_1561-84del
XR_001744858.1:n.1561-86_1561-84del
NM_001354609.2:c.1433-86_1433-84del	NP_001341538.1:n.1433-86_1433-84del
NM_001374244.1:c.1553-86_1553-84del	NP_001361173.1:n.1553-86_1553-84del
NM_001374258.1:c.1553-86_1553-84del MANE Plus Clinical	NP_001361187.1:n.1553-86_1553-84del
NM_004333.6:c.1433-86_1433-84del MANE Select	NP_004324.2:n.1433-86_1433-84del
NM_001378467.1:c.1442-86_1442-84del	NP_001365396.1:n.1442-86_1442-84del
NM_001378468.1:c.1433-86_1433-84del	NP_001365397.1:n.1433-86_1433-84del
NM_001378469.1:c.1367-86_1367-84del	NP_001365398.1:n.1367-86_1367-84del
NM_001378470.1:c.1331-86_1331-84del	NP_001365399.1:n.1331-86_1331-84del
NM_001378471.1:c.1322-86_1322-84del	NP_001365400.1:n.1322-86_1322-84del
NM_001378472.1:c.1277-86_1277-84del	NP_001365401.1:n.1277-86_1277-84del
NM_001378473.1:c.1277-86_1277-84del	NP_001365402.1:n.1277-86_1277-84del
NM_001378474.1:c.1433-86_1433-84del	NP_001365403.1:n.1433-86_1433-84del
NM_001378475.1:c.1169-86_1169-84del	NP_001365404.1:n.1169-86_1169-84del