Canonical Allele Identifier: CA834246465

Gene: BRAF

Linked Data

• dbSNP Id: rs1338524212
• gnomAD v3: 7-140755200-GTA-G
• gnomAD v4: 7-140755200-GTA-G
• MyVariant Identifiers: chr7:g.140455001_140455002del (hg19) ; chr7:g.140755201_140755202del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140755202_140755203del , CM000669.2:g.140755202_140755203del	GRCh38
NC_000007.13:g.140455002_140455003del , CM000669.1:g.140455002_140455003del	GRCh37
NC_000007.12:g.140101471_140101472del	NCBI36
NG_007873.3:g.174563_174564del , LRG_299:g.174563_174564del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1695-969_1695-968del MANE Select	ENSP00000493543.1:n.1695-969_1695-968del
ENST00000288602.11:c.1815-969_1815-968del	ENSP00000288602.7:n.1815-969_1815-968del
ENST00000479537.6:c.365-969_365-968del
ENST00000496384.7:c.1695-969_1695-968del	ENSP00000419060.2:n.1695-969_1695-968del
ENST00000497784.2:c.*1145-969_*1145-968del	ENSP00000420119.2:n.*1145-969_*1145-968del
ENST00000642228.1:c.*773-969_*773-968del	ENSP00000493678.1:n.*773-969_*773-968del
ENST00000642875.1:n.1259-5784_1259-5783del
ENST00000644120.1:n.2085-969_2085-968del
ENST00000644650.1:c.791-969_791-968del
ENST00000644905.1:n.1784-969_1784-968del
ENST00000644969.2:c.1815-969_1815-968del MANE Plus Clinical	ENSP00000496776.1:n.1815-969_1815-968del
ENST00000646730.1:c.*271-969_*271-968del	ENSP00000494784.1:n.*271-969_*271-968del
ENST00000646891.1:c.1695-969_1695-968del	ENSP00000493543.1:n.1695-969_1695-968del
ENST00000647434.1:c.738-5784_738-5783del	ENSP00000495132.1:n.738-5784_738-5783del
ENST00000288602.10:c.1695-969_1695-968del	ENSP00000288602.6:n.1695-969_1695-968del
ENST00000496384.6:c.518-969_518-968del
ENST00000497784.1:c.1730-969_1730-968del	ENSP00000420119.1:n.1730-969_1730-968del
NM_004333.4:c.1695-969_1695-968del , LRG_299t1:c.1695-969_1695-968del	NP_004324.2:n.1695-969_1695-968del
XM_005250045.1:c.1695-969_1695-968del	XP_005250102.1:n.1695-969_1695-968del
XM_005250046.1:c.1695-969_1695-968del	XP_005250103.1:n.1695-969_1695-968del
XM_011516529.1:c.1695-969_1695-968del	XP_011514831.1:n.1695-969_1695-968del
XM_011516530.1:c.1695-5784_1695-5783del	XP_011514832.1:n.1695-5784_1695-5783del
XR_242190.1:n.1703-969_1703-968del
XR_927520.1:n.1703-969_1703-968del
XR_927521.1:n.1703-969_1703-968del
XR_927522.1:n.1703-5784_1703-5783del
XR_927523.1:n.1703-5784_1703-5783del
NM_001354609.1:c.1695-969_1695-968del	NP_001341538.1:n.1695-969_1695-968del
NM_004333.5:c.1695-969_1695-968del	NP_004324.2:n.1695-969_1695-968del
NR_148928.1:n.2000-969_2000-968del
XM_017012558.1:c.1815-969_1815-968del	XP_016868047.1:n.1815-969_1815-968del
XM_017012559.1:c.1815-969_1815-968del	XP_016868048.1:n.1815-969_1815-968del
XR_001744857.1:n.1823-969_1823-968del
XR_001744858.1:n.1823-5784_1823-5783del
NM_001354609.2:c.1695-969_1695-968del	NP_001341538.1:n.1695-969_1695-968del
NM_001374244.1:c.1815-969_1815-968del	NP_001361173.1:n.1815-969_1815-968del
NM_001374258.1:c.1815-969_1815-968del MANE Plus Clinical	NP_001361187.1:n.1815-969_1815-968del
NM_004333.6:c.1695-969_1695-968del MANE Select	NP_004324.2:n.1695-969_1695-968del
NM_001378467.1:c.1704-969_1704-968del	NP_001365396.1:n.1704-969_1704-968del
NM_001378468.1:c.1695-969_1695-968del	NP_001365397.1:n.1695-969_1695-968del
NM_001378469.1:c.1629-969_1629-968del	NP_001365398.1:n.1629-969_1629-968del
NM_001378470.1:c.1593-969_1593-968del	NP_001365399.1:n.1593-969_1593-968del
NM_001378471.1:c.1584-969_1584-968del	NP_001365400.1:n.1584-969_1584-968del
NM_001378472.1:c.1539-969_1539-968del	NP_001365401.1:n.1539-969_1539-968del
NM_001378473.1:c.1539-969_1539-968del	NP_001365402.1:n.1539-969_1539-968del
NM_001378474.1:c.1695-969_1695-968del	NP_001365403.1:n.1695-969_1695-968del
NM_001378475.1:c.1431-969_1431-968del	NP_001365404.1:n.1431-969_1431-968del