Canonical Allele Identifier: CA1747732053

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140800379_140800396delinsGGGTGCGGAAGGGGATGA , CM000669.2:g.140800379_140800396delinsGGGTGCGGAAGGGGATGA	GRCh38
NC_000007.13:g.140500179_140500196delinsGGGTGCGGAAGGGGATGA , CM000669.1:g.140500179_140500196delinsGGGTGCGGAAGGGGATGA	GRCh37
NC_000007.12:g.140146648_140146665delinsGGGTGCGGAAGGGGATGA	NCBI36
NG_007873.3:g.129369_129386delinsTCATCCCCTTCCGCACCC , LRG_299:g.129369_129386delinsTCATCCCCTTCCGCACCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.946_963delinsTCATCCCCTTCCGCACCC MANE Select	ENSP00000493543.1:p.Ser316=
ENST00000288602.11:c.946_963delinsTCATCCCCTTCCGCACCC	ENSP00000288602.7:p.Ser316=
ENST00000496384.7:c.946_963delinsTCATCCCCTTCCGCACCC	ENSP00000419060.2:p.Ser316=
ENST00000497784.2:c.*396_*413delinsTCATCCCCTTCCGCACCC	ENSP00000420119.2:n.*396_*413delinsTCATCCCCTTCCGCACCC
ENST00000642228.1:c.*24_*41delinsTCATCCCCTTCCGCACCC	ENSP00000493678.1:n.*24_*41delinsTCATCCCCTTCCGCACCC
ENST00000642272.1:n.978_995delinsTCATCCCCTTCCGCACCC
ENST00000642875.1:n.440_457delinsTCATCCCCTTCCGCACCC
ENST00000644120.1:n.1388_1405delinsTCATCCCCTTCCGCACCC
ENST00000644650.1:c.42_59delinsTCATCCCCTTCCGCACCC
ENST00000644905.1:n.1035_1052delinsTCATCCCCTTCCGCACCC
ENST00000644969.2:c.946_963delinsTCATCCCCTTCCGCACCC MANE Plus Clinical	ENSP00000496776.1:p.Ser316=
ENST00000646730.1:c.946_963delinsTCATCCCCTTCCGCACCC	ENSP00000494784.1:p.Ser316=
ENST00000646891.1:c.946_963delinsTCATCCCCTTCCGCACCC	ENSP00000493543.1:p.Ser316=
ENST00000288602.10:c.946_963delinsTCATCCCCTTCCGCACCC	ENSP00000288602.6:p.Ser316=
ENST00000497784.1:c.981_998delinsTCATCCCCTTCCGCACCC	ENSP00000420119.1:n.981_998delinsTCATCCCCTTCCGCACCC
NM_004333.4:c.946_963delinsTCATCCCCTTCCGCACCC , LRG_299t1:c.946_963delinsTCATCCCCTTCCGCACCC	NP_004324.2:p.Ser316=
XM_005250045.1:c.946_963delinsTCATCCCCTTCCGCACCC	XP_005250102.1:p.Ser316=
XM_005250046.1:c.946_963delinsTCATCCCCTTCCGCACCC	XP_005250103.1:p.Ser316=
XM_011516529.1:c.946_963delinsTCATCCCCTTCCGCACCC	XP_011514831.1:p.Ser316=
XM_011516530.1:c.946_963delinsTCATCCCCTTCCGCACCC	XP_011514832.1:p.Ser316=
XR_242190.1:n.954_971delinsTCATCCCCTTCCGCACCC
XR_927520.1:n.954_971delinsTCATCCCCTTCCGCACCC
XR_927521.1:n.954_971delinsTCATCCCCTTCCGCACCC
XR_927522.1:n.954_971delinsTCATCCCCTTCCGCACCC
XR_927523.1:n.954_971delinsTCATCCCCTTCCGCACCC
NM_001354609.1:c.946_963delinsTCATCCCCTTCCGCACCC	NP_001341538.1:p.Ser316=
NM_004333.5:c.946_963delinsTCATCCCCTTCCGCACCC	NP_004324.2:p.Ser316=
NR_148928.1:n.1251_1268delinsTCATCCCCTTCCGCACCC
XM_017012558.1:c.946_963delinsTCATCCCCTTCCGCACCC	XP_016868047.1:p.Ser316=
XM_017012559.1:c.946_963delinsTCATCCCCTTCCGCACCC	XP_016868048.1:p.Ser316=
XR_001744857.1:n.954_971delinsTCATCCCCTTCCGCACCC
XR_001744858.1:n.954_971delinsTCATCCCCTTCCGCACCC
NM_001354609.2:c.946_963delinsTCATCCCCTTCCGCACCC	NP_001341538.1:p.Ser316=
NM_001374244.1:c.946_963delinsTCATCCCCTTCCGCACCC	NP_001361173.1:p.Ser316=
NM_001374258.1:c.946_963delinsTCATCCCCTTCCGCACCC MANE Plus Clinical	NP_001361187.1:p.Ser316=
NM_004333.6:c.946_963delinsTCATCCCCTTCCGCACCC MANE Select	NP_004324.2:p.Ser316=
NM_001378467.1:c.955_972delinsTCATCCCCTTCCGCACCC	NP_001365396.1:p.Ser319=
NM_001378468.1:c.946_963delinsTCATCCCCTTCCGCACCC	NP_001365397.1:p.Ser316=
NM_001378469.1:c.946_963delinsTCATCCCCTTCCGCACCC	NP_001365398.1:p.Ser316=
NM_001378470.1:c.844_861delinsTCATCCCCTTCCGCACCC	NP_001365399.1:p.Ser282=
NM_001378471.1:c.946_963delinsTCATCCCCTTCCGCACCC	NP_001365400.1:p.Ser316=
NM_001378472.1:c.790_807delinsTCATCCCCTTCCGCACCC	NP_001365401.1:p.Ser264=
NM_001378473.1:c.790_807delinsTCATCCCCTTCCGCACCC	NP_001365402.1:p.Ser264=
NM_001378474.1:c.946_963delinsTCATCCCCTTCCGCACCC	NP_001365403.1:p.Ser316=
NM_001378475.1:c.682_699delinsTCATCCCCTTCCGCACCC	NP_001365404.1:p.Ser228=