Canonical Allele Identifier: CA16602427
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 375948
dbSNP Id: rs1057519718
COSMIC: COSM211600

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753355_140753356delinsTC , CM000669.2:g.140753355_140753356delinsTC GRCh38
NC_000007.13:g.140453155_140453156delinsTC , CM000669.1:g.140453155_140453156delinsTC GRCh37
NC_000007.12:g.140099624_140099625delinsTC NCBI36
NG_007873.3:g.176409_176410delinsGA , LRG_299:g.176409_176410delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000288602.11:c.1899_1900delinsGA ENSP00000288602.7:p.Asp634Asn
ENST00000479537.6:n.449_450delinsGA
ENST00000496384.7:c.1779_1780delinsGA ENSP00000419060.2:p.Asp594Asn
ENST00000497784.2:c.*1229_*1230delinsGA ENSP00000420119.2:p.=
ENST00000642228.1:c.*857_*858delinsGA ENSP00000493678.1:p.=
ENST00000642875.1:n.1259-3938_1259-3937delinsGA
ENST00000644120.1:n.2169_2170delinsGA
ENST00000644650.1:n.875_876delinsGA
ENST00000644905.1:n.2661_2662delinsGA
ENST00000644969.2:c.1899_1900delinsGA MANE Select ENSP00000496776.1:p.Asp634Asn
ENST00000646730.1:c.*355_*356delinsGA ENSP00000494784.1:p.=
ENST00000646891.1:c.1779_1780delinsGA ENSP00000493543.1:p.Asp594Asn
ENST00000647434.1:n.738-3938_738-3937delinsGA ENSP00000495132.1:p.=
ENST00000288602.10:c.1779_1780delinsGA ENSP00000288602.6:p.Asp594Asn
ENST00000479537.5:n.63_64delinsGA ENSP00000418033.1:p.Asp22Asn
ENST00000496384.6:n.602_603delinsGA
ENST00000497784.1:n.1814_1815delinsGA ENSP00000420119.1:p.=
NM_004333.4:c.1779_1780delinsGA , LRG_299t1:c.1779_1780delinsGA NP_004324.2:p.Asp594Asn
XM_005250045.1:c.1779_1780delinsGA XP_005250102.1:p.Asp594Asn
XM_005250046.1:c.1779_1780delinsGA XP_005250103.1:p.Asp594Asn
XM_011516529.1:c.1779_1780delinsGA XP_011514831.1:p.Asp594Asn
XM_011516530.1:c.1695-3938_1695-3937delinsGA XP_011514832.1:p.=
XR_242190.1:n.1787_1788delinsGA
XR_927520.1:n.1787_1788delinsGA
XR_927521.1:n.1787_1788delinsGA
XR_927522.1:n.1703-3938_1703-3937delinsGA
XR_927523.1:n.1703-3938_1703-3937delinsGA
NM_001354609.1:c.1779_1780delinsGA NP_001341538.1:p.Asp594Asn
NM_004333.5:c.1779_1780delinsGA NP_004324.2:p.Asp594Asn
NR_148928.1:n.2877_2878delinsGA
XM_017012558.1:c.1899_1900delinsGA XP_016868047.1:p.Asp634Asn
XM_017012559.1:c.1899_1900delinsGA XP_016868048.1:p.Asp634Asn
XR_001744857.1:n.1907_1908delinsGA
XR_001744858.1:n.1823-3938_1823-3937delinsGA
NM_001354609.2:c.1779_1780delinsGA NP_001341538.1:p.Asp594Asn
NM_001374244.1:c.1899_1900delinsGA NP_001361173.1:p.Asp634Asn
NM_001374258.1:c.1899_1900delinsGA MANE Select NP_001361187.1:p.Asp634Asn
NM_004333.6:c.1779_1780delinsGA NP_004324.2:p.Asp594Asn
NM_001378467.1:c.1788_1789delinsGA NP_001365396.1:p.Asp597Asn
NM_001378468.1:c.1779_1780delinsGA NP_001365397.1:p.Asp594Asn
NM_001378469.1:c.1713_1714delinsGA NP_001365398.1:p.Asp572Asn
NM_001378470.1:c.1677_1678delinsGA NP_001365399.1:p.Asp560Asn
NM_001378471.1:c.1668_1669delinsGA NP_001365400.1:p.Asp557Asn
NM_001378472.1:c.1623_1624delinsGA NP_001365401.1:p.Asp542Asn
NM_001378473.1:c.1623_1624delinsGA NP_001365402.1:p.Asp542Asn
NM_001378474.1:c.1779_1780delinsGA NP_001365403.1:p.Asp594Asn
NM_001378475.1:c.1515_1516delinsGA NP_001365404.1:p.Asp506Asn