Canonical Allele Identifier: CA1747710064
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753460_140753461delinsGT , CM000669.2:g.140753460_140753461delinsGT GRCh38
NC_000007.13:g.140453260_140453261delinsGT , CM000669.1:g.140453260_140453261delinsGT GRCh37
NC_000007.12:g.140099729_140099730delinsGT NCBI36
NG_007873.3:g.176304_176305delinsAC , LRG_299:g.176304_176305delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1742-68_1742-67delinsAC MANE Select ENSP00000493543.1:n.1742-68_1742-67delinsAC
ENST00000288602.11:c.1862-68_1862-67delinsAC ENSP00000288602.7:n.1862-68_1862-67delinsAC
ENST00000479537.6:c.412-68_412-67delinsAC
ENST00000496384.7:c.1742-68_1742-67delinsAC ENSP00000419060.2:n.1742-68_1742-67delinsAC
ENST00000497784.2:c.*1192-68_*1192-67delinsAC ENSP00000420119.2:n.*1192-68_*1192-67delinsAC
ENST00000642228.1:c.*820-68_*820-67delinsAC ENSP00000493678.1:n.*820-68_*820-67delinsAC
ENST00000642875.1:n.1259-4043_1259-4042delinsAC
ENST00000644120.1:n.2132-68_2132-67delinsAC
ENST00000644650.1:c.838-68_838-67delinsAC
ENST00000644905.1:n.2556_2557delinsAC
ENST00000644969.2:c.1862-68_1862-67delinsAC MANE Plus Clinical ENSP00000496776.1:n.1862-68_1862-67delinsAC
ENST00000646730.1:c.*318-68_*318-67delinsAC ENSP00000494784.1:n.*318-68_*318-67delinsAC
ENST00000646891.1:c.1742-68_1742-67delinsAC ENSP00000493543.1:n.1742-68_1742-67delinsAC
ENST00000647434.1:c.738-4043_738-4042delinsAC ENSP00000495132.1:n.738-4043_738-4042delinsAC
ENST00000288602.10:c.1742-68_1742-67delinsAC ENSP00000288602.6:n.1742-68_1742-67delinsAC
ENST00000479537.5:c.26-68_26-67delinsAC ENSP00000418033.1:n.26-68_26-67delinsAC
ENST00000496384.6:c.565-68_565-67delinsAC
ENST00000497784.1:c.1777-68_1777-67delinsAC ENSP00000420119.1:n.1777-68_1777-67delinsAC
NM_004333.4:c.1742-68_1742-67delinsAC , LRG_299t1:c.1742-68_1742-67delinsAC NP_004324.2:n.1742-68_1742-67delinsAC
XM_005250045.1:c.1742-68_1742-67delinsAC XP_005250102.1:n.1742-68_1742-67delinsAC
XM_005250046.1:c.1742-68_1742-67delinsAC XP_005250103.1:n.1742-68_1742-67delinsAC
XM_011516529.1:c.1742-68_1742-67delinsAC XP_011514831.1:n.1742-68_1742-67delinsAC
XM_011516530.1:c.1695-4043_1695-4042delinsAC XP_011514832.1:n.1695-4043_1695-4042delinsAC
XR_242190.1:n.1750-68_1750-67delinsAC
XR_927520.1:n.1750-68_1750-67delinsAC
XR_927521.1:n.1750-68_1750-67delinsAC
XR_927522.1:n.1703-4043_1703-4042delinsAC
XR_927523.1:n.1703-4043_1703-4042delinsAC
NM_001354609.1:c.1742-68_1742-67delinsAC NP_001341538.1:n.1742-68_1742-67delinsAC
NM_004333.5:c.1742-68_1742-67delinsAC NP_004324.2:n.1742-68_1742-67delinsAC
NR_148928.1:n.2772_2773delinsAC
XM_017012558.1:c.1862-68_1862-67delinsAC XP_016868047.1:n.1862-68_1862-67delinsAC
XM_017012559.1:c.1862-68_1862-67delinsAC XP_016868048.1:n.1862-68_1862-67delinsAC
XR_001744857.1:n.1870-68_1870-67delinsAC
XR_001744858.1:n.1823-4043_1823-4042delinsAC
NM_001354609.2:c.1742-68_1742-67delinsAC NP_001341538.1:n.1742-68_1742-67delinsAC
NM_001374244.1:c.1862-68_1862-67delinsAC NP_001361173.1:n.1862-68_1862-67delinsAC
NM_001374258.1:c.1862-68_1862-67delinsAC MANE Plus Clinical NP_001361187.1:n.1862-68_1862-67delinsAC
NM_004333.6:c.1742-68_1742-67delinsAC MANE Select NP_004324.2:n.1742-68_1742-67delinsAC
NM_001378467.1:c.1751-68_1751-67delinsAC NP_001365396.1:n.1751-68_1751-67delinsAC
NM_001378468.1:c.1742-68_1742-67delinsAC NP_001365397.1:n.1742-68_1742-67delinsAC
NM_001378469.1:c.1676-68_1676-67delinsAC NP_001365398.1:n.1676-68_1676-67delinsAC
NM_001378470.1:c.1640-68_1640-67delinsAC NP_001365399.1:n.1640-68_1640-67delinsAC
NM_001378471.1:c.1631-68_1631-67delinsAC NP_001365400.1:n.1631-68_1631-67delinsAC
NM_001378472.1:c.1586-68_1586-67delinsAC NP_001365401.1:n.1586-68_1586-67delinsAC
NM_001378473.1:c.1586-68_1586-67delinsAC NP_001365402.1:n.1586-68_1586-67delinsAC
NM_001378474.1:c.1742-68_1742-67delinsAC NP_001365403.1:n.1742-68_1742-67delinsAC
NM_001378475.1:c.1478-68_1478-67delinsAC NP_001365404.1:n.1478-68_1478-67delinsAC