Canonical Allele Identifier: CA1747725999
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140777037T= , CM000669.2:g.140777037T= GRCh38
NC_000007.13:g.140476837T= , CM000669.1:g.140476837T= GRCh37
NC_000007.12:g.140123306T= NCBI36
NG_007873.3:g.152728A= , LRG_299:g.152728A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1569A= MANE Select ENSP00000493543.1:p.Pro523=
ENST00000288602.11:c.1689A= ENSP00000288602.7:p.Pro563=
ENST00000479537.6:c.239A=
ENST00000496384.7:c.1569A= ENSP00000419060.2:p.Pro523=
ENST00000497784.2:c.*1019A= ENSP00000420119.2:n.*1019A=
ENST00000642228.1:c.*647A= ENSP00000493678.1:n.*647A=
ENST00000642875.1:n.1133A=
ENST00000644120.1:n.1959A=
ENST00000644650.1:c.665A=
ENST00000644905.1:n.1658A=
ENST00000644969.2:c.1689A= MANE Plus Clinical ENSP00000496776.1:p.Pro563=
ENST00000646730.1:c.1569A= ENSP00000494784.1:p.Pro523=
ENST00000646891.1:c.1569A= ENSP00000493543.1:p.Pro523=
ENST00000647434.1:c.612A= ENSP00000495132.1:p.Pro204=
ENST00000288602.10:c.1569A= ENSP00000288602.6:p.Pro523=
ENST00000496384.6:c.392A=
ENST00000497784.1:c.1604A= ENSP00000420119.1:n.1604A=
NM_004333.4:c.1569A= , LRG_299t1:c.1569A= NP_004324.2:p.Pro523=
XM_005250045.1:c.1569A= XP_005250102.1:p.Pro523=
XM_005250046.1:c.1569A= XP_005250103.1:p.Pro523=
XM_011516529.1:c.1569A= XP_011514831.1:p.Pro523=
XM_011516530.1:c.1569A= XP_011514832.1:p.Pro523=
XR_242190.1:n.1577A=
XR_927520.1:n.1577A=
XR_927521.1:n.1577A=
XR_927522.1:n.1577A=
XR_927523.1:n.1577A=
NM_001354609.1:c.1569A= NP_001341538.1:p.Pro523=
NM_004333.5:c.1569A= NP_004324.2:p.Pro523=
NR_148928.1:n.1874A=
XM_017012558.1:c.1689A= XP_016868047.1:p.Pro563=
XM_017012559.1:c.1689A= XP_016868048.1:p.Pro563=
XR_001744857.1:n.1697A=
XR_001744858.1:n.1697A=
NM_001354609.2:c.1569A= NP_001341538.1:p.Pro523=
NM_001374244.1:c.1689A= NP_001361173.1:p.Pro563=
NM_001374258.1:c.1689A= MANE Plus Clinical NP_001361187.1:p.Pro563=
NM_004333.6:c.1569A= MANE Select NP_004324.2:p.Pro523=
NM_001378467.1:c.1578A= NP_001365396.1:p.Pro526=
NM_001378468.1:c.1569A= NP_001365397.1:p.Pro523=
NM_001378469.1:c.1503A= NP_001365398.1:p.Pro501=
NM_001378470.1:c.1467A= NP_001365399.1:p.Pro489=
NM_001378471.1:c.1458A= NP_001365400.1:p.Pro486=
NM_001378472.1:c.1413A= NP_001365401.1:p.Pro471=
NM_001378473.1:c.1413A= NP_001365402.1:p.Pro471=
NM_001378474.1:c.1569A= NP_001365403.1:p.Pro523=
NM_001378475.1:c.1305A= NP_001365404.1:p.Pro435=