Canonical Allele Identifier: CA168154740

Gene: BRAF

Linked Data

• dbSNP Id: rs1027897772
• MyVariant Identifiers: chr7:g.140592163_140592168del (hg19) ; chr7:g.140892363_140892368del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140892363_140892368del , CM000669.2:g.140892363_140892368del	GRCh38
NC_000007.13:g.140592163_140592168del , CM000669.1:g.140592163_140592168del	GRCh37
NC_000007.12:g.140238632_140238637del	NCBI36
NG_007873.3:g.37397_37402del , LRG_299:g.37397_37402del

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.138+32198_138+32203del MANE Select	ENSP00000493543.1:n.138+32198_138+32203de...
ENST00000288602.11:c.138+32198_138+32203del	ENSP00000288602.7:n.138+32198_138+32203de...
ENST00000469930.2:c.138+32198_138+32203del	ENSP00000495858.1:n.138+32198_138+32203de...
ENST00000496384.7:c.138+32198_138+32203del	ENSP00000419060.2:n.138+32198_138+32203de...
ENST00000497784.2:c.138+32198_138+32203del	ENSP00000420119.2:n.138+32198_138+32203de...
ENST00000642228.1:c.138+32198_138+32203del	ENSP00000493678.1:n.138+32198_138+32203de...
ENST00000642272.1:n.161+32198_161+32203del
ENST00000642808.1:n.138+32198_138+32203del
ENST00000643790.1:n.141+32198_141+32203del
ENST00000644905.1:n.147+32198_147+32203del
ENST00000644969.2:c.138+32198_138+32203del MANE Plus Clinical	ENSP00000496776.1:n.138+32198_138+32203de...
ENST00000646730.1:c.138+32198_138+32203del	ENSP00000494784.1:n.138+32198_138+32203de...
ENST00000646891.1:c.138+32198_138+32203del	ENSP00000493543.1:n.138+32198_138+32203de...
ENST00000288602.10:c.138+32198_138+32203del	ENSP00000288602.6:n.138+32198_138+32203de...
ENST00000469930.1:n.144+32198_144+32203del
ENST00000497784.1:c.93+32198_93+32203del	ENSP00000420119.1:n.93+32198_93+32203del
NM_004333.4:c.138+32198_138+32203del , LRG_299t1:c.138+32198_138+32203del	NP_004324.2:n.138+32198_138+32203del
XM_005250045.1:c.138+32198_138+32203del	XP_005250102.1:n.138+32198_138+32203del
XM_005250046.1:c.138+32198_138+32203del	XP_005250103.1:n.138+32198_138+32203del
XM_011516529.1:c.138+32198_138+32203del	XP_011514831.1:n.138+32198_138+32203del
XM_011516530.1:c.138+32198_138+32203del	XP_011514832.1:n.138+32198_138+32203del
XR_242190.1:n.146+32198_146+32203del
XR_927520.1:n.146+32198_146+32203del
XR_927521.1:n.146+32198_146+32203del
XR_927522.1:n.146+32198_146+32203del
XR_927523.1:n.146+32198_146+32203del
NM_001354609.1:c.138+32198_138+32203del	NP_001341538.1:n.138+32198_138+32203del
NM_004333.5:c.138+32198_138+32203del	NP_004324.2:n.138+32198_138+32203del
NR_148928.1:n.363+32198_363+32203del
XM_017012558.1:c.138+32198_138+32203del	XP_016868047.1:n.138+32198_138+32203del
XM_017012559.1:c.138+32198_138+32203del	XP_016868048.1:n.138+32198_138+32203del
XR_001744857.1:n.146+32198_146+32203del
XR_001744858.1:n.146+32198_146+32203del
NM_001354609.2:c.138+32198_138+32203del	NP_001341538.1:n.138+32198_138+32203del
NM_001374244.1:c.138+32198_138+32203del	NP_001361173.1:n.138+32198_138+32203del
NM_001374258.1:c.138+32198_138+32203del MANE Plus Clinical	NP_001361187.1:n.138+32198_138+32203del
NM_004333.6:c.138+32198_138+32203del MANE Select	NP_004324.2:n.138+32198_138+32203del
NM_001378467.1:c.138+32198_138+32203del	NP_001365396.1:n.138+32198_138+32203del
NM_001378468.1:c.138+32198_138+32203del	NP_001365397.1:n.138+32198_138+32203del
NM_001378469.1:c.138+32198_138+32203del	NP_001365398.1:n.138+32198_138+32203del
NM_001378470.1:c.138+32198_138+32203del	NP_001365399.1:n.138+32198_138+32203del
NM_001378471.1:c.138+32198_138+32203del	NP_001365400.1:n.138+32198_138+32203del
NM_001378472.1:c.-19+31818_-19+31823del	NP_001365401.1:n.-19+31818_-19+31823del
NM_001378473.1:c.-19+31818_-19+31823del	NP_001365402.1:n.-19+31818_-19+31823del
NM_001378474.1:c.138+32198_138+32203del	NP_001365403.1:n.138+32198_138+32203del
NM_001378475.1:c.138+32198_138+32203del	NP_001365404.1:n.138+32198_138+32203del