Canonical Allele Identifier: CA645544101
Gene: BRAF HGNC NCBI

Linked Data

COSMIC: COSM26504

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753338_140753355dup , CM000669.2:g.140753338_140753355dup GRCh38
NC_000007.13:g.140453138_140453155dup , CM000669.1:g.140453138_140453155dup GRCh37
NC_000007.12:g.140099607_140099624dup NCBI36
NG_007873.3:g.176411_176428dup , LRG_299:g.176411_176428dup

Transcript Alleles

HGVS Amino-acid change
ENST00000288602.11:c.1901_1918dup ENSP00000288602.7:p.Thr639_Val640insAspPh...
ENST00000479537.6:n.451_468dup
ENST00000496384.7:c.1781_1798dup ENSP00000419060.2:p.Thr599_Val600insAspPh...
ENST00000497784.2:c.*1231_*1248dup ENSP00000420119.2:p.=
ENST00000642228.1:c.*859_*876dup ENSP00000493678.1:p.=
ENST00000642875.1:n.1259-3936_1259-3919dup
ENST00000644120.1:n.2171_2188dup
ENST00000644650.1:n.877_894dup
ENST00000644905.1:n.2663_2680dup
ENST00000644969.2:c.1901_1918dup MANE Select ENSP00000496776.1:p.Thr639_Val640insAspPh...
ENST00000646730.1:c.*357_*374dup ENSP00000494784.1:p.=
ENST00000646891.1:c.1781_1798dup ENSP00000493543.1:p.Thr599_Val600insAspPh...
ENST00000647434.1:n.738-3936_738-3919dup ENSP00000495132.1:p.=
ENST00000288602.10:c.1781_1798dup ENSP00000288602.6:p.Thr599_Val600insAspPh...
ENST00000479537.5:n.65_82dup ENSP00000418033.1:p.Thr27_Val28insAspPheG...
ENST00000496384.6:n.604_621dup
ENST00000497784.1:n.1816_1833dup ENSP00000420119.1:p.=
NM_004333.4:c.1781_1798dup , LRG_299t1:c.1781_1798dup NP_004324.2:p.Thr599_Val600insAspPheGlyLe...
XM_005250045.1:c.1781_1798dup XP_005250102.1:p.Thr599_Val600insAspPheGl...
XM_005250046.1:c.1781_1798dup XP_005250103.1:p.Thr599_Val600insAspPheGl...
XM_011516529.1:c.1781_1798dup XP_011514831.1:p.Thr599_Val600insAspPheGl...
XM_011516530.1:c.1695-3936_1695-3919dup XP_011514832.1:p.=
XR_242190.1:n.1789_1806dup
XR_927520.1:n.1789_1806dup
XR_927521.1:n.1789_1806dup
XR_927522.1:n.1703-3936_1703-3919dup
XR_927523.1:n.1703-3936_1703-3919dup
NM_001354609.1:c.1781_1798dup NP_001341538.1:p.Thr599_Val600insAspPheGl...
NM_004333.5:c.1781_1798dup NP_004324.2:p.Thr599_Val600insAspPheGlyLe...
NR_148928.1:n.2879_2896dup
XM_017012558.1:c.1901_1918dup XP_016868047.1:p.Thr639_Val640insAspPheGl...
XM_017012559.1:c.1901_1918dup XP_016868048.1:p.Thr639_Val640insAspPheGl...
XR_001744857.1:n.1909_1926dup
XR_001744858.1:n.1823-3936_1823-3919dup
NM_001354609.2:c.1781_1798dup NP_001341538.1:p.Thr599_Val600insAspPheGl...
NM_001374244.1:c.1901_1918dup NP_001361173.1:p.Thr639_Val640insAspPheGl...
NM_001374258.1:c.1901_1918dup MANE Select NP_001361187.1:p.Thr639_Val640insAspPheGl...
NM_004333.6:c.1781_1798dup NP_004324.2:p.Thr599_Val600insAspPheGlyLe...
NM_001378467.1:c.1790_1807dup NP_001365396.1:p.Thr602_Val603insAspPheGl...
NM_001378468.1:c.1781_1798dup NP_001365397.1:p.Thr599_Val600insAspPheGl...
NM_001378469.1:c.1715_1732dup NP_001365398.1:p.Thr577_Val578insAspPheGl...
NM_001378470.1:c.1679_1696dup NP_001365399.1:p.Thr565_Val566insAspPheGl...
NM_001378471.1:c.1670_1687dup NP_001365400.1:p.Thr562_Val563insAspPheGl...
NM_001378472.1:c.1625_1642dup NP_001365401.1:p.Thr547_Val548insAspPheGl...
NM_001378473.1:c.1625_1642dup NP_001365402.1:p.Thr547_Val548insAspPheGl...
NM_001378474.1:c.1781_1798dup NP_001365403.1:p.Thr599_Val600insAspPheGl...
NM_001378475.1:c.1517_1534dup NP_001365404.1:p.Thr511_Val512insAspPheGl...