Canonical Allele Identifier: CA578401841

Gene: BRAF

Linked Data

• dbSNP Id: rs563291402
• gnomAD v2: 7-140592055-C-CAA
• gnomAD v3: 7-140892255-C-CAA
• gnomAD v4: 7-140892255-C-CAA
• MyVariant Identifiers: chr7:g.140592057_140592058insAA (hg19) ; chr7:g.140592055_140592056insAA (hg19) ; chr7:g.140892257_140892258insAA (hg38) ; chr7:g.140892255_140892256insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140892266_140892267dup , CM000669.2:g.140892266_140892267dup	GRCh38
NC_000007.13:g.140592066_140592067dup , CM000669.1:g.140592066_140592067dup	GRCh37
NC_000007.12:g.140238535_140238536dup	NCBI36
NG_007873.3:g.37508_37509dup , LRG_299:g.37508_37509dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.138+32309_138+32310dup MANE Select	ENSP00000493543.1:n.138+32309_138+32310dup
ENST00000288602.11:c.138+32309_138+32310dup	ENSP00000288602.7:n.138+32309_138+32310dup
ENST00000469930.2:c.138+32309_138+32310dup	ENSP00000495858.1:n.138+32309_138+32310dup
ENST00000496384.7:c.138+32309_138+32310dup	ENSP00000419060.2:n.138+32309_138+32310dup
ENST00000497784.2:c.138+32309_138+32310dup	ENSP00000420119.2:n.138+32309_138+32310dup
ENST00000642228.1:c.138+32309_138+32310dup	ENSP00000493678.1:n.138+32309_138+32310dup
ENST00000642272.1:n.161+32309_161+32310dup
ENST00000642808.1:n.138+32309_138+32310dup
ENST00000643790.1:n.141+32309_141+32310dup
ENST00000644905.1:n.147+32309_147+32310dup
ENST00000644969.2:c.138+32309_138+32310dup MANE Plus Clinical	ENSP00000496776.1:n.138+32309_138+32310dup
ENST00000646730.1:c.138+32309_138+32310dup	ENSP00000494784.1:n.138+32309_138+32310dup
ENST00000646891.1:c.138+32309_138+32310dup	ENSP00000493543.1:n.138+32309_138+32310dup
ENST00000288602.10:c.138+32309_138+32310dup	ENSP00000288602.6:n.138+32309_138+32310dup
ENST00000469930.1:n.144+32309_144+32310dup
ENST00000497784.1:c.93+32309_93+32310dup	ENSP00000420119.1:n.93+32309_93+32310dup
NM_004333.4:c.138+32309_138+32310dup , LRG_299t1:c.138+32309_138+32310dup	NP_004324.2:n.138+32309_138+32310dup
XM_005250045.1:c.138+32309_138+32310dup	XP_005250102.1:n.138+32309_138+32310dup
XM_005250046.1:c.138+32309_138+32310dup	XP_005250103.1:n.138+32309_138+32310dup
XM_011516529.1:c.138+32309_138+32310dup	XP_011514831.1:n.138+32309_138+32310dup
XM_011516530.1:c.138+32309_138+32310dup	XP_011514832.1:n.138+32309_138+32310dup
XR_242190.1:n.146+32309_146+32310dup
XR_927520.1:n.146+32309_146+32310dup
XR_927521.1:n.146+32309_146+32310dup
XR_927522.1:n.146+32309_146+32310dup
XR_927523.1:n.146+32309_146+32310dup
NM_001354609.1:c.138+32309_138+32310dup	NP_001341538.1:n.138+32309_138+32310dup
NM_004333.5:c.138+32309_138+32310dup	NP_004324.2:n.138+32309_138+32310dup
NR_148928.1:n.363+32309_363+32310dup
XM_017012558.1:c.138+32309_138+32310dup	XP_016868047.1:n.138+32309_138+32310dup
XM_017012559.1:c.138+32309_138+32310dup	XP_016868048.1:n.138+32309_138+32310dup
XR_001744857.1:n.146+32309_146+32310dup
XR_001744858.1:n.146+32309_146+32310dup
NM_001354609.2:c.138+32309_138+32310dup	NP_001341538.1:n.138+32309_138+32310dup
NM_001374244.1:c.138+32309_138+32310dup	NP_001361173.1:n.138+32309_138+32310dup
NM_001374258.1:c.138+32309_138+32310dup MANE Plus Clinical	NP_001361187.1:n.138+32309_138+32310dup
NM_004333.6:c.138+32309_138+32310dup MANE Select	NP_004324.2:n.138+32309_138+32310dup
NM_001378467.1:c.138+32309_138+32310dup	NP_001365396.1:n.138+32309_138+32310dup
NM_001378468.1:c.138+32309_138+32310dup	NP_001365397.1:n.138+32309_138+32310dup
NM_001378469.1:c.138+32309_138+32310dup	NP_001365398.1:n.138+32309_138+32310dup
NM_001378470.1:c.138+32309_138+32310dup	NP_001365399.1:n.138+32309_138+32310dup
NM_001378471.1:c.138+32309_138+32310dup	NP_001365400.1:n.138+32309_138+32310dup
NM_001378472.1:c.-19+31929_-19+31930dup	NP_001365401.1:n.-19+31929_-19+31930dup
NM_001378473.1:c.-19+31929_-19+31930dup	NP_001365402.1:n.-19+31929_-19+31930dup
NM_001378474.1:c.138+32309_138+32310dup	NP_001365403.1:n.138+32309_138+32310dup
NM_001378475.1:c.138+32309_138+32310dup	NP_001365404.1:n.138+32309_138+32310dup