Canonical Allele Identifier: CA891842036
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753354_140753357delinsCCAG , CM000669.2:g.140753354_140753357delinsCCAG GRCh38
NC_000007.13:g.140453154_140453157delinsCCAG , CM000669.1:g.140453154_140453157delinsCCAG GRCh37
NC_000007.12:g.140099623_140099626delinsCCAG NCBI36
NG_007873.3:g.176408_176411delinsCTGG , LRG_299:g.176408_176411delinsCTGG

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1778_1781delinsCTGG MANE Select ENSP00000493543.1:p.Gly593_Asp594delinsAl...
ENST00000288602.11:c.1898_1901delinsCTGG ENSP00000288602.7:p.Gly633_Asp634delinsAl...
ENST00000479537.6:c.448_451delinsCTGG
ENST00000496384.7:c.1778_1781delinsCTGG ENSP00000419060.2:p.Gly593_Asp594delinsAl...
ENST00000497784.2:c.*1228_*1231delinsCTGG ENSP00000420119.2:n.*1228_*1231delinsCTGG...
ENST00000642228.1:c.*856_*859delinsCTGG ENSP00000493678.1:n.*856_*859delinsCTGG
ENST00000642875.1:n.1259-3939_1259-3936delinsCTGG
ENST00000644120.1:n.2168_2171delinsCTGG
ENST00000644650.1:c.874_877delinsCTGG
ENST00000644905.1:n.2660_2663delinsCTGG
ENST00000644969.2:c.1898_1901delinsCTGG MANE Plus Clinical ENSP00000496776.1:p.Gly633_Asp634delinsAl...
ENST00000646730.1:c.*354_*357delinsCTGG ENSP00000494784.1:n.*354_*357delinsCTGG
ENST00000646891.1:c.1778_1781delinsCTGG ENSP00000493543.1:p.Gly593_Asp594delinsAl...
ENST00000647434.1:c.738-3939_738-3936delinsCTGG ENSP00000495132.1:n.738-3939_738-3936deli...
ENST00000288602.10:c.1778_1781delinsCTGG ENSP00000288602.6:p.Gly593_Asp594delinsAl...
ENST00000479537.5:c.62_65delinsCTGG ENSP00000418033.1:p.Gly21_Asp22delinsAlaG...
ENST00000496384.6:c.601_604delinsCTGG
ENST00000497784.1:c.1813_1816delinsCTGG ENSP00000420119.1:n.1813_1816delinsCTGG
NM_004333.4:c.1778_1781delinsCTGG , LRG_299t1:c.1778_1781delinsCTGG NP_004324.2:p.Gly593_Asp594delinsAlaGly
XM_005250045.1:c.1778_1781delinsCTGG XP_005250102.1:p.Gly593_Asp594delinsAlaGl...
XM_005250046.1:c.1778_1781delinsCTGG XP_005250103.1:p.Gly593_Asp594delinsAlaGl...
XM_011516529.1:c.1778_1781delinsCTGG XP_011514831.1:p.Gly593_Asp594delinsAlaGl...
XM_011516530.1:c.1695-3939_1695-3936delinsCTGG XP_011514832.1:n.1695-3939_1695-3936delin...
XR_242190.1:n.1786_1789delinsCTGG
XR_927520.1:n.1786_1789delinsCTGG
XR_927521.1:n.1786_1789delinsCTGG
XR_927522.1:n.1703-3939_1703-3936delinsCTGG
XR_927523.1:n.1703-3939_1703-3936delinsCTGG
NM_001354609.1:c.1778_1781delinsCTGG NP_001341538.1:p.Gly593_Asp594delinsAlaGl...
NM_004333.5:c.1778_1781delinsCTGG NP_004324.2:p.Gly593_Asp594delinsAlaGly
NR_148928.1:n.2876_2879delinsCTGG
XM_017012558.1:c.1898_1901delinsCTGG XP_016868047.1:p.Gly633_Asp634delinsAlaGl...
XM_017012559.1:c.1898_1901delinsCTGG XP_016868048.1:p.Gly633_Asp634delinsAlaGl...
XR_001744857.1:n.1906_1909delinsCTGG
XR_001744858.1:n.1823-3939_1823-3936delinsCTGG
NM_001354609.2:c.1778_1781delinsCTGG NP_001341538.1:p.Gly593_Asp594delinsAlaGl...
NM_001374244.1:c.1898_1901delinsCTGG NP_001361173.1:p.Gly633_Asp634delinsAlaGl...
NM_001374258.1:c.1898_1901delinsCTGG MANE Plus Clinical NP_001361187.1:p.Gly633_Asp634delinsAlaGl...
NM_004333.6:c.1778_1781delinsCTGG MANE Select NP_004324.2:p.Gly593_Asp594delinsAlaGly
NM_001378467.1:c.1787_1790delinsCTGG NP_001365396.1:p.Gly596_Asp597delinsAlaGl...
NM_001378468.1:c.1778_1781delinsCTGG NP_001365397.1:p.Gly593_Asp594delinsAlaGl...
NM_001378469.1:c.1712_1715delinsCTGG NP_001365398.1:p.Gly571_Asp572delinsAlaGl...
NM_001378470.1:c.1676_1679delinsCTGG NP_001365399.1:p.Gly559_Asp560delinsAlaGl...
NM_001378471.1:c.1667_1670delinsCTGG NP_001365400.1:p.Gly556_Asp557delinsAlaGl...
NM_001378472.1:c.1622_1625delinsCTGG NP_001365401.1:p.Gly541_Asp542delinsAlaGl...
NM_001378473.1:c.1622_1625delinsCTGG NP_001365402.1:p.Gly541_Asp542delinsAlaGl...
NM_001378474.1:c.1778_1781delinsCTGG NP_001365403.1:p.Gly593_Asp594delinsAlaGl...
NM_001378475.1:c.1514_1517delinsCTGG NP_001365404.1:p.Gly505_Asp506delinsAlaGl...