Canonical Allele Identifier: CA1747732068

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140800399_140800404delinsCAGATG , CM000669.2:g.140800399_140800404delinsCAGATG	GRCh38
NC_000007.13:g.140500199_140500204delinsCAGATG , CM000669.1:g.140500199_140500204delinsCAGATG	GRCh37
NC_000007.12:g.140146668_140146673delinsCAGATG	NCBI36
NG_007873.3:g.129361_129366delinsCATCTG , LRG_299:g.129361_129366delinsCATCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.938_943delinsCATCTG MANE Select	ENSP00000493543.1:p.Thr313=
ENST00000288602.11:c.938_943delinsCATCTG	ENSP00000288602.7:p.Thr313=
ENST00000496384.7:c.938_943delinsCATCTG	ENSP00000419060.2:p.Thr313=
ENST00000497784.2:c.*388_*393delinsCATCTG	ENSP00000420119.2:n.*388_*393delinsCATCTG
ENST00000642228.1:c.*16_*21delinsCATCTG	ENSP00000493678.1:n.*16_*21delinsCATCTG
ENST00000642272.1:n.970_975delinsCATCTG
ENST00000642875.1:n.432_437delinsCATCTG
ENST00000644120.1:n.1380_1385delinsCATCTG
ENST00000644650.1:c.34_39delinsCATCTG
ENST00000644905.1:n.1027_1032delinsCATCTG
ENST00000644969.2:c.938_943delinsCATCTG MANE Plus Clinical	ENSP00000496776.1:p.Thr313=
ENST00000646730.1:c.938_943delinsCATCTG	ENSP00000494784.1:p.Thr313=
ENST00000646891.1:c.938_943delinsCATCTG	ENSP00000493543.1:p.Thr313=
ENST00000288602.10:c.938_943delinsCATCTG	ENSP00000288602.6:p.Thr313=
ENST00000497784.1:c.973_978delinsCATCTG	ENSP00000420119.1:n.973_978delinsCATCTG
NM_004333.4:c.938_943delinsCATCTG , LRG_299t1:c.938_943delinsCATCTG	NP_004324.2:p.Thr313=
XM_005250045.1:c.938_943delinsCATCTG	XP_005250102.1:p.Thr313=
XM_005250046.1:c.938_943delinsCATCTG	XP_005250103.1:p.Thr313=
XM_011516529.1:c.938_943delinsCATCTG	XP_011514831.1:p.Thr313=
XM_011516530.1:c.938_943delinsCATCTG	XP_011514832.1:p.Thr313=
XR_242190.1:n.946_951delinsCATCTG
XR_927520.1:n.946_951delinsCATCTG
XR_927521.1:n.946_951delinsCATCTG
XR_927522.1:n.946_951delinsCATCTG
XR_927523.1:n.946_951delinsCATCTG
NM_001354609.1:c.938_943delinsCATCTG	NP_001341538.1:p.Thr313=
NM_004333.5:c.938_943delinsCATCTG	NP_004324.2:p.Thr313=
NR_148928.1:n.1243_1248delinsCATCTG
XM_017012558.1:c.938_943delinsCATCTG	XP_016868047.1:p.Thr313=
XM_017012559.1:c.938_943delinsCATCTG	XP_016868048.1:p.Thr313=
XR_001744857.1:n.946_951delinsCATCTG
XR_001744858.1:n.946_951delinsCATCTG
NM_001354609.2:c.938_943delinsCATCTG	NP_001341538.1:p.Thr313=
NM_001374244.1:c.938_943delinsCATCTG	NP_001361173.1:p.Thr313=
NM_001374258.1:c.938_943delinsCATCTG MANE Plus Clinical	NP_001361187.1:p.Thr313=
NM_004333.6:c.938_943delinsCATCTG MANE Select	NP_004324.2:p.Thr313=
NM_001378467.1:c.947_952delinsCATCTG	NP_001365396.1:p.Thr316=
NM_001378468.1:c.938_943delinsCATCTG	NP_001365397.1:p.Thr313=
NM_001378469.1:c.938_943delinsCATCTG	NP_001365398.1:p.Thr313=
NM_001378470.1:c.836_841delinsCATCTG	NP_001365399.1:p.Thr279=
NM_001378471.1:c.938_943delinsCATCTG	NP_001365400.1:p.Thr313=
NM_001378472.1:c.782_787delinsCATCTG	NP_001365401.1:p.Thr261=
NM_001378473.1:c.782_787delinsCATCTG	NP_001365402.1:p.Thr261=
NM_001378474.1:c.938_943delinsCATCTG	NP_001365403.1:p.Thr313=
NM_001378475.1:c.674_679delinsCATCTG	NP_001365404.1:p.Thr225=