Canonical Allele Identifier: CA2580077575
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711072
ClinVar RCV Id: RCV002292359

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753357_140753358insATC , CM000669.2:g.140753357_140753358insATC GRCh38
NC_000007.13:g.140453157_140453158insATC , CM000669.1:g.140453157_140453158insATC GRCh37
NC_000007.12:g.140099626_140099627insATC NCBI36
NG_007873.3:g.176408_176409insATG , LRG_299:g.176408_176409insATG

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1778_1779insATG MANE Select ENSP00000493543.1:p.Gly593_Asp594insCys
ENST00000288602.11:c.1898_1899insATG ENSP00000288602.7:p.Gly633_Asp634insCys
ENST00000479537.6:c.448_449insATG
ENST00000496384.7:c.1778_1779insATG ENSP00000419060.2:p.Gly593_Asp594insCys
ENST00000497784.2:c.*1228_*1229insATG ENSP00000420119.2:n.*1228_*1229insATG
ENST00000642228.1:c.*856_*857insATG ENSP00000493678.1:n.*856_*857insATG
ENST00000642875.1:n.1259-3939_1259-3938insATG
ENST00000644120.1:n.2168_2169insATG
ENST00000644650.1:c.874_875insATG
ENST00000644905.1:n.2660_2661insATG
ENST00000644969.2:c.1898_1899insATG MANE Plus Clinical ENSP00000496776.1:p.Gly633_Asp634insCys
ENST00000646730.1:c.*354_*355insATG ENSP00000494784.1:n.*354_*355insATG
ENST00000646891.1:c.1778_1779insATG ENSP00000493543.1:p.Gly593_Asp594insCys
ENST00000647434.1:c.738-3939_738-3938insATG ENSP00000495132.1:n.738-3939_738-3938insA...
ENST00000288602.10:c.1778_1779insATG ENSP00000288602.6:p.Gly593_Asp594insCys
ENST00000479537.5:c.62_63insATG ENSP00000418033.1:p.Gly21_Asp22insCys
ENST00000496384.6:c.601_602insATG
ENST00000497784.1:c.1813_1814insATG ENSP00000420119.1:n.1813_1814insATG
NM_004333.4:c.1778_1779insATG , LRG_299t1:c.1778_1779insATG NP_004324.2:p.Gly593_Asp594insCys
XM_005250045.1:c.1778_1779insATG XP_005250102.1:p.Gly593_Asp594insCys
XM_005250046.1:c.1778_1779insATG XP_005250103.1:p.Gly593_Asp594insCys
XM_011516529.1:c.1778_1779insATG XP_011514831.1:p.Gly593_Asp594insCys
XM_011516530.1:c.1695-3939_1695-3938insATG XP_011514832.1:n.1695-3939_1695-3938insAT...
XR_242190.1:n.1786_1787insATG
XR_927520.1:n.1786_1787insATG
XR_927521.1:n.1786_1787insATG
XR_927522.1:n.1703-3939_1703-3938insATG
XR_927523.1:n.1703-3939_1703-3938insATG
NM_001354609.1:c.1778_1779insATG NP_001341538.1:p.Gly593_Asp594insCys
NM_004333.5:c.1778_1779insATG NP_004324.2:p.Gly593_Asp594insCys
NR_148928.1:n.2876_2877insATG
XM_017012558.1:c.1898_1899insATG XP_016868047.1:p.Gly633_Asp634insCys
XM_017012559.1:c.1898_1899insATG XP_016868048.1:p.Gly633_Asp634insCys
XR_001744857.1:n.1906_1907insATG
XR_001744858.1:n.1823-3939_1823-3938insATG
NM_001354609.2:c.1778_1779insATG NP_001341538.1:p.Gly593_Asp594insCys
NM_001374244.1:c.1898_1899insATG NP_001361173.1:p.Gly633_Asp634insCys
NM_001374258.1:c.1898_1899insATG MANE Plus Clinical NP_001361187.1:p.Gly633_Asp634insCys
NM_004333.6:c.1778_1779insATG MANE Select NP_004324.2:p.Gly593_Asp594insCys
NM_001378467.1:c.1787_1788insATG NP_001365396.1:p.Gly596_Asp597insCys
NM_001378468.1:c.1778_1779insATG NP_001365397.1:p.Gly593_Asp594insCys
NM_001378469.1:c.1712_1713insATG NP_001365398.1:p.Gly571_Asp572insCys
NM_001378470.1:c.1676_1677insATG NP_001365399.1:p.Gly559_Asp560insCys
NM_001378471.1:c.1667_1668insATG NP_001365400.1:p.Gly556_Asp557insCys
NM_001378472.1:c.1622_1623insATG NP_001365401.1:p.Gly541_Asp542insCys
NM_001378473.1:c.1622_1623insATG NP_001365402.1:p.Gly541_Asp542insCys
NM_001378474.1:c.1778_1779insATG NP_001365403.1:p.Gly593_Asp594insCys
NM_001378475.1:c.1514_1515insATG NP_001365404.1:p.Gly505_Asp506insCys