Canonical Allele Identifier: CA645556778
Gene: BRAF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781592_140781600dup , CM000669.2:g.140781592_140781600dup GRCh38
NC_000007.13:g.140481392_140481400dup , CM000669.1:g.140481392_140481400dup GRCh37
NC_000007.12:g.140127861_140127869dup NCBI36
NG_007873.3:g.148166_148174dup , LRG_299:g.148166_148174dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1409_1417dup MANE Select ENSP00000493543.1:p.Tyr472_Lys473insThrValTyr
ENST00000288602.11:c.1529_1537dup ENSP00000288602.7:p.Tyr512_Lys513insThrValTyr
ENST00000479537.6:c.79_87dup
ENST00000496384.7:c.1409_1417dup ENSP00000419060.2:p.Tyr472_Lys473insThrValTyr
ENST00000497784.2:c.*859_*867dup ENSP00000420119.2:n.*859_*867dup
ENST00000642228.1:c.*487_*495dup ENSP00000493678.1:n.*487_*495dup
ENST00000642875.1:n.851_859dup
ENST00000644120.1:n.1799_1807dup
ENST00000644650.1:c.505_513dup
ENST00000644905.1:n.1498_1506dup
ENST00000644969.2:c.1529_1537dup MANE Plus Clinical ENSP00000496776.1:p.Tyr512_Lys513insThrValTyr
ENST00000646334.1:n.539_547dup
ENST00000646730.1:c.1409_1417dup ENSP00000494784.1:p.Tyr472_Lys473insThrValTyr
ENST00000646891.1:c.1409_1417dup ENSP00000493543.1:p.Tyr472_Lys473insThrValTyr
ENST00000647434.1:c.452_460dup ENSP00000495132.1:p.Tyr153_Lys154insThrValTyr
ENST00000288602.10:c.1409_1417dup ENSP00000288602.6:p.Tyr472_Lys473insThrValTyr
ENST00000496384.6:c.232_240dup
ENST00000497784.1:c.1444_1452dup ENSP00000420119.1:n.1444_1452dup
NM_004333.4:c.1409_1417dup , LRG_299t1:c.1409_1417dup NP_004324.2:p.Tyr472_Lys473insThrValTyr
XM_005250045.1:c.1409_1417dup XP_005250102.1:p.Tyr472_Lys473insThrValTyr
XM_005250046.1:c.1409_1417dup XP_005250103.1:p.Tyr472_Lys473insThrValTyr
XM_011516529.1:c.1409_1417dup XP_011514831.1:p.Tyr472_Lys473insThrValTyr
XM_011516530.1:c.1409_1417dup XP_011514832.1:p.Tyr472_Lys473insThrValTyr
XR_242190.1:n.1417_1425dup
XR_927520.1:n.1417_1425dup
XR_927521.1:n.1417_1425dup
XR_927522.1:n.1417_1425dup
XR_927523.1:n.1417_1425dup
NM_001354609.1:c.1409_1417dup NP_001341538.1:p.Tyr472_Lys473insThrValTyr
NM_004333.5:c.1409_1417dup NP_004324.2:p.Tyr472_Lys473insThrValTyr
NR_148928.1:n.1714_1722dup
XM_017012558.1:c.1529_1537dup XP_016868047.1:p.Tyr512_Lys513insThrValTyr
XM_017012559.1:c.1529_1537dup XP_016868048.1:p.Tyr512_Lys513insThrValTyr
XR_001744857.1:n.1537_1545dup
XR_001744858.1:n.1537_1545dup
NM_001354609.2:c.1409_1417dup NP_001341538.1:p.Tyr472_Lys473insThrValTyr
NM_001374244.1:c.1529_1537dup NP_001361173.1:p.Tyr512_Lys513insThrValTyr
NM_001374258.1:c.1529_1537dup MANE Plus Clinical NP_001361187.1:p.Tyr512_Lys513insThrValTyr
NM_004333.6:c.1409_1417dup MANE Select NP_004324.2:p.Tyr472_Lys473insThrValTyr
NM_001378467.1:c.1418_1426dup NP_001365396.1:p.Tyr475_Lys476insThrValTyr
NM_001378468.1:c.1409_1417dup NP_001365397.1:p.Tyr472_Lys473insThrValTyr
NM_001378469.1:c.1343_1351dup NP_001365398.1:p.Tyr450_Lys451insThrValTyr
NM_001378470.1:c.1307_1315dup NP_001365399.1:p.Tyr438_Lys439insThrValTyr
NM_001378471.1:c.1298_1306dup NP_001365400.1:p.Tyr435_Lys436insThrValTyr
NM_001378472.1:c.1253_1261dup NP_001365401.1:p.Tyr420_Lys421insThrValTyr
NM_001378473.1:c.1253_1261dup NP_001365402.1:p.Tyr420_Lys421insThrValTyr
NM_001378474.1:c.1409_1417dup NP_001365403.1:p.Tyr472_Lys473insThrValTyr
NM_001378475.1:c.1145_1153dup NP_001365404.1:p.Tyr384_Lys385insThrValTyr