Canonical Allele Identifier: CA369542769
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs2128998133

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753289A>T , CM000669.2:g.140753289A>T GRCh38
NC_000007.13:g.140453089A>T , CM000669.1:g.140453089A>T GRCh37
NC_000007.12:g.140099558A>T NCBI36
NG_007873.3:g.176476T>A , LRG_299:g.176476T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1846T>A MANE Select ENSP00000493543.1:p.Ser616Thr
ENST00000288602.11:c.1966T>A ENSP00000288602.7:p.Ser656Thr
ENST00000479537.6:c.516T>A
ENST00000496384.7:c.1846T>A ENSP00000419060.2:p.Ser616Thr
ENST00000497784.2:c.*1296T>A ENSP00000420119.2:n.*1296T>A
ENST00000642228.1:c.*924T>A ENSP00000493678.1:n.*924T>A
ENST00000642875.1:n.1259-3871T>A
ENST00000644120.1:n.2236T>A
ENST00000644650.1:c.942T>A
ENST00000644905.1:n.2728T>A
ENST00000644969.2:c.1966T>A MANE Plus Clinical ENSP00000496776.1:p.Ser656Thr
ENST00000646730.1:c.*422T>A ENSP00000494784.1:n.*422T>A
ENST00000646891.1:c.1846T>A ENSP00000493543.1:p.Ser616Thr
ENST00000647434.1:c.738-3871T>A ENSP00000495132.1:n.738-3871T>A
ENST00000288602.10:c.1846T>A ENSP00000288602.6:p.Ser616Thr
ENST00000479537.5:c.130T>A ENSP00000418033.1:p.Ser44Thr
ENST00000496384.6:c.669T>A
ENST00000497784.1:c.1881T>A ENSP00000420119.1:n.1881T>A
NM_004333.4:c.1846T>A , LRG_299t1:c.1846T>A NP_004324.2:p.Ser616Thr
XM_005250045.1:c.1846T>A XP_005250102.1:p.Ser616Thr
XM_005250046.1:c.1846T>A XP_005250103.1:p.Ser616Thr
XM_011516529.1:c.1846T>A XP_011514831.1:p.Ser616Thr
XM_011516530.1:c.1695-3871T>A XP_011514832.1:n.1695-3871T>A
XR_242190.1:n.1854T>A
XR_927520.1:n.1854T>A
XR_927521.1:n.1854T>A
XR_927522.1:n.1703-3871T>A
XR_927523.1:n.1703-3871T>A
NM_001354609.1:c.1846T>A NP_001341538.1:p.Ser616Thr
NM_004333.5:c.1846T>A NP_004324.2:p.Ser616Thr
NR_148928.1:n.2944T>A
XM_017012558.1:c.1966T>A XP_016868047.1:p.Ser656Thr
XM_017012559.1:c.1966T>A XP_016868048.1:p.Ser656Thr
XR_001744857.1:n.1974T>A
XR_001744858.1:n.1823-3871T>A
NM_001354609.2:c.1846T>A NP_001341538.1:p.Ser616Thr
NM_001374244.1:c.1966T>A NP_001361173.1:p.Ser656Thr
NM_001374258.1:c.1966T>A MANE Plus Clinical NP_001361187.1:p.Ser656Thr
NM_004333.6:c.1846T>A MANE Select NP_004324.2:p.Ser616Thr
NM_001378467.1:c.1855T>A NP_001365396.1:p.Ser619Thr
NM_001378468.1:c.1846T>A NP_001365397.1:p.Ser616Thr
NM_001378469.1:c.1780T>A NP_001365398.1:p.Ser594Thr
NM_001378470.1:c.1744T>A NP_001365399.1:p.Ser582Thr
NM_001378471.1:c.1735T>A NP_001365400.1:p.Ser579Thr
NM_001378472.1:c.1690T>A NP_001365401.1:p.Ser564Thr
NM_001378473.1:c.1690T>A NP_001365402.1:p.Ser564Thr
NM_001378474.1:c.1846T>A NP_001365403.1:p.Ser616Thr
NM_001378475.1:c.1582T>A NP_001365404.1:p.Ser528Thr