Canonical Allele Identifier: CA645544086

Gene: BRAF

Linked Data

• COSMIC: COSM4172019

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753324_140753335del , CM000669.2:g.140753324_140753335del	GRCh38
NC_000007.13:g.140453124_140453135del , CM000669.1:g.140453124_140453135del	GRCh37
NC_000007.12:g.140099593_140099604del	NCBI36
NG_007873.3:g.176432_176443del , LRG_299:g.176432_176443del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1802_1813del MANE Select	ENSP00000493543.1:p.Lys601_Trp604del
ENST00000288602.11:c.1922_1933del	ENSP00000288602.7:p.Lys641_Trp644del
ENST00000479537.6:c.472_483del
ENST00000496384.7:c.1802_1813del	ENSP00000419060.2:p.Lys601_Trp604del
ENST00000497784.2:c.*1252_*1263del	ENSP00000420119.2:n.*1252_*1263del
ENST00000642228.1:c.*880_*891del	ENSP00000493678.1:n.*880_*891del
ENST00000642875.1:n.1259-3915_1259-3904del
ENST00000644120.1:n.2192_2203del
ENST00000644650.1:c.898_909del
ENST00000644905.1:n.2684_2695del
ENST00000644969.2:c.1922_1933del MANE Plus Clinical	ENSP00000496776.1:p.Lys641_Trp644del
ENST00000646730.1:c.*378_*389del	ENSP00000494784.1:n.*378_*389del
ENST00000646891.1:c.1802_1813del	ENSP00000493543.1:p.Lys601_Trp604del
ENST00000647434.1:c.738-3915_738-3904del	ENSP00000495132.1:n.738-3915_738-3904del
ENST00000288602.10:c.1802_1813del	ENSP00000288602.6:p.Lys601_Trp604del
ENST00000479537.5:c.86_97del	ENSP00000418033.1:p.Lys29_Trp32del
ENST00000496384.6:c.625_636del
ENST00000497784.1:c.1837_1848del	ENSP00000420119.1:n.1837_1848del
NM_004333.4:c.1802_1813del , LRG_299t1:c.1802_1813del	NP_004324.2:p.Lys601_Trp604del
XM_005250045.1:c.1802_1813del	XP_005250102.1:p.Lys601_Trp604del
XM_005250046.1:c.1802_1813del	XP_005250103.1:p.Lys601_Trp604del
XM_011516529.1:c.1802_1813del	XP_011514831.1:p.Lys601_Trp604del
XM_011516530.1:c.1695-3915_1695-3904del	XP_011514832.1:n.1695-3915_1695-3904del
XR_242190.1:n.1810_1821del
XR_927520.1:n.1810_1821del
XR_927521.1:n.1810_1821del
XR_927522.1:n.1703-3915_1703-3904del
XR_927523.1:n.1703-3915_1703-3904del
NM_001354609.1:c.1802_1813del	NP_001341538.1:p.Lys601_Trp604del
NM_004333.5:c.1802_1813del	NP_004324.2:p.Lys601_Trp604del
NR_148928.1:n.2900_2911del
XM_017012558.1:c.1922_1933del	XP_016868047.1:p.Lys641_Trp644del
XM_017012559.1:c.1922_1933del	XP_016868048.1:p.Lys641_Trp644del
XR_001744857.1:n.1930_1941del
XR_001744858.1:n.1823-3915_1823-3904del
NM_001354609.2:c.1802_1813del	NP_001341538.1:p.Lys601_Trp604del
NM_001374244.1:c.1922_1933del	NP_001361173.1:p.Lys641_Trp644del
NM_001374258.1:c.1922_1933del MANE Plus Clinical	NP_001361187.1:p.Lys641_Trp644del
NM_004333.6:c.1802_1813del MANE Select	NP_004324.2:p.Lys601_Trp604del
NM_001378467.1:c.1811_1822del	NP_001365396.1:p.Lys604_Trp607del
NM_001378468.1:c.1802_1813del	NP_001365397.1:p.Lys601_Trp604del
NM_001378469.1:c.1736_1747del	NP_001365398.1:p.Lys579_Trp582del
NM_001378470.1:c.1700_1711del	NP_001365399.1:p.Lys567_Trp570del
NM_001378471.1:c.1691_1702del	NP_001365400.1:p.Lys564_Trp567del
NM_001378472.1:c.1646_1657del	NP_001365401.1:p.Lys549_Trp552del
NM_001378473.1:c.1646_1657del	NP_001365402.1:p.Lys549_Trp552del
NM_001378474.1:c.1802_1813del	NP_001365403.1:p.Lys601_Trp604del
NM_001378475.1:c.1538_1549del	NP_001365404.1:p.Lys513_Trp516del