Canonical Allele Identifier: CA1747732079
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140800420C= , CM000669.2:g.140800420C= GRCh38
NC_000007.13:g.140500220C= , CM000669.1:g.140500220C= GRCh37
NC_000007.12:g.140146689C= NCBI36
NG_007873.3:g.129345G= , LRG_299:g.129345G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.922G= MANE Select ENSP00000493543.1:p.Ala308=
ENST00000288602.11:c.922G= ENSP00000288602.7:p.Ala308=
ENST00000496384.7:c.922G= ENSP00000419060.2:p.Ala308=
ENST00000497784.2:c.*372G= ENSP00000420119.2:n.*372G=
ENST00000642228.1:c.903G= ENSP00000493678.1:p.Ter301=
ENST00000642272.1:n.954G=
ENST00000642875.1:n.416G=
ENST00000644120.1:n.1364G=
ENST00000644650.1:c.18G=
ENST00000644905.1:n.1011G=
ENST00000644969.2:c.922G= MANE Plus Clinical ENSP00000496776.1:p.Ala308=
ENST00000646730.1:c.922G= ENSP00000494784.1:p.Ala308=
ENST00000646891.1:c.922G= ENSP00000493543.1:p.Ala308=
ENST00000288602.10:c.922G= ENSP00000288602.6:p.Ala308=
ENST00000497784.1:c.957G= ENSP00000420119.1:n.957G=
NM_004333.4:c.922G= , LRG_299t1:c.922G= NP_004324.2:p.Ala308=
XM_005250045.1:c.922G= XP_005250102.1:p.Ala308=
XM_005250046.1:c.922G= XP_005250103.1:p.Ala308=
XM_011516529.1:c.922G= XP_011514831.1:p.Ala308=
XM_011516530.1:c.922G= XP_011514832.1:p.Ala308=
XR_242190.1:n.930G=
XR_927520.1:n.930G=
XR_927521.1:n.930G=
XR_927522.1:n.930G=
XR_927523.1:n.930G=
NM_001354609.1:c.922G= NP_001341538.1:p.Ala308=
NM_004333.5:c.922G= NP_004324.2:p.Ala308=
NR_148928.1:n.1227G=
XM_017012558.1:c.922G= XP_016868047.1:p.Ala308=
XM_017012559.1:c.922G= XP_016868048.1:p.Ala308=
XR_001744857.1:n.930G=
XR_001744858.1:n.930G=
NM_001354609.2:c.922G= NP_001341538.1:p.Ala308=
NM_001374244.1:c.922G= NP_001361173.1:p.Ala308=
NM_001374258.1:c.922G= MANE Plus Clinical NP_001361187.1:p.Ala308=
NM_004333.6:c.922G= MANE Select NP_004324.2:p.Ala308=
NM_001378467.1:c.931G= NP_001365396.1:p.Ala311=
NM_001378468.1:c.922G= NP_001365397.1:p.Ala308=
NM_001378469.1:c.922G= NP_001365398.1:p.Ala308=
NM_001378470.1:c.820G= NP_001365399.1:p.Ala274=
NM_001378471.1:c.922G= NP_001365400.1:p.Ala308=
NM_001378472.1:c.766G= NP_001365401.1:p.Ala256=
NM_001378473.1:c.766G= NP_001365402.1:p.Ala256=
NM_001378474.1:c.922G= NP_001365403.1:p.Ala308=
NM_001378475.1:c.658G= NP_001365404.1:p.Ala220=