Canonical Allele Identifier: CA834245045

Gene: BRAF

Linked Data

• dbSNP Id: rs1359307237
• gnomAD v3: 7-140753010-ATTTAT-A
• gnomAD v4: 7-140753010-ATTTAT-A
• MyVariant Identifiers: chr7:g.140452811_140452815del (hg19) ; chr7:g.140753011_140753015del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753013_140753017del , CM000669.2:g.140753013_140753017del	GRCh38
NC_000007.13:g.140452813_140452817del , CM000669.1:g.140452813_140452817del	GRCh37
NC_000007.12:g.140099282_140099286del	NCBI36
NG_007873.3:g.176750_176754del , LRG_299:g.176750_176754del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1860+260_1860+264del MANE Select	ENSP00000493543.1:n.1860+260_1860+264del
ENST00000288602.11:c.1980+260_1980+264del	ENSP00000288602.7:n.1980+260_1980+264del
ENST00000479537.6:c.530+260_530+264del
ENST00000496384.7:c.1860+260_1860+264del	ENSP00000419060.2:n.1860+260_1860+264del
ENST00000497784.2:c.*1310+260_*1310+264del	ENSP00000420119.2:n.*1310+260_*1310+264del
ENST00000642228.1:c.*938+260_*938+264del	ENSP00000493678.1:n.*938+260_*938+264del
ENST00000642875.1:n.1259-3597_1259-3593del
ENST00000644120.1:n.2250+260_2250+264del
ENST00000644650.1:c.956+260_956+264del
ENST00000644905.1:n.2742+260_2742+264del
ENST00000644969.2:c.1980+260_1980+264del MANE Plus Clinical	ENSP00000496776.1:n.1980+260_1980+264del
ENST00000646730.1:c.*436+260_*436+264del	ENSP00000494784.1:n.*436+260_*436+264del
ENST00000646891.1:c.1860+260_1860+264del	ENSP00000493543.1:n.1860+260_1860+264del
ENST00000647434.1:c.738-3597_738-3593del	ENSP00000495132.1:n.738-3597_738-3593del
ENST00000288602.10:c.1860+260_1860+264del	ENSP00000288602.6:n.1860+260_1860+264del
ENST00000479537.5:c.144+260_144+264del	ENSP00000418033.1:n.144+260_144+264del
ENST00000496384.6:c.683+260_683+264del
ENST00000497784.1:c.1895+260_1895+264del	ENSP00000420119.1:n.1895+260_1895+264del
NM_004333.4:c.1860+260_1860+264del , LRG_299t1:c.1860+260_1860+264del	NP_004324.2:n.1860+260_1860+264del
XM_005250045.1:c.1860+260_1860+264del	XP_005250102.1:n.1860+260_1860+264del
XM_005250046.1:c.1860+260_1860+264del	XP_005250103.1:n.1860+260_1860+264del
XM_011516529.1:c.1860+260_1860+264del	XP_011514831.1:n.1860+260_1860+264del
XM_011516530.1:c.1695-3597_1695-3593del	XP_011514832.1:n.1695-3597_1695-3593del
XR_242190.1:n.1868+260_1868+264del
XR_927520.1:n.1868+260_1868+264del
XR_927521.1:n.1868+260_1868+264del
XR_927522.1:n.1703-3597_1703-3593del
XR_927523.1:n.1703-3597_1703-3593del
NM_001354609.1:c.1860+260_1860+264del	NP_001341538.1:n.1860+260_1860+264del
NM_004333.5:c.1860+260_1860+264del	NP_004324.2:n.1860+260_1860+264del
NR_148928.1:n.2958+260_2958+264del
XM_017012558.1:c.1980+260_1980+264del	XP_016868047.1:n.1980+260_1980+264del
XM_017012559.1:c.1980+260_1980+264del	XP_016868048.1:n.1980+260_1980+264del
XR_001744857.1:n.1988+260_1988+264del
XR_001744858.1:n.1823-3597_1823-3593del
NM_001354609.2:c.1860+260_1860+264del	NP_001341538.1:n.1860+260_1860+264del
NM_001374244.1:c.1980+260_1980+264del	NP_001361173.1:n.1980+260_1980+264del
NM_001374258.1:c.1980+260_1980+264del MANE Plus Clinical	NP_001361187.1:n.1980+260_1980+264del
NM_004333.6:c.1860+260_1860+264del MANE Select	NP_004324.2:n.1860+260_1860+264del
NM_001378467.1:c.1869+260_1869+264del	NP_001365396.1:n.1869+260_1869+264del
NM_001378468.1:c.1860+260_1860+264del	NP_001365397.1:n.1860+260_1860+264del
NM_001378469.1:c.1794+260_1794+264del	NP_001365398.1:n.1794+260_1794+264del
NM_001378470.1:c.1758+260_1758+264del	NP_001365399.1:n.1758+260_1758+264del
NM_001378471.1:c.1749+260_1749+264del	NP_001365400.1:n.1749+260_1749+264del
NM_001378472.1:c.1704+260_1704+264del	NP_001365401.1:n.1704+260_1704+264del
NM_001378473.1:c.1704+260_1704+264del	NP_001365402.1:n.1704+260_1704+264del
NM_001378474.1:c.1860+260_1860+264del	NP_001365403.1:n.1860+260_1860+264del
NM_001378475.1:c.1596+260_1596+264del	NP_001365404.1:n.1596+260_1596+264del