Canonical Allele Identifier: CA2715969585

Gene: BRAF

Linked Data

• dbSNP Id: rs2129018499

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140777043del , CM000669.2:g.140777043del	GRCh38
NC_000007.13:g.140476843del , CM000669.1:g.140476843del	GRCh37
NC_000007.12:g.140123312del	NCBI36
NG_007873.3:g.152724del , LRG_299:g.152724del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1565del MANE Select	ENSP00000493543.1:p.Lys522SerfsTer29
ENST00000288602.11:c.1685del	ENSP00000288602.7:p.Lys562SerfsTer29
ENST00000479537.6:c.235del
ENST00000496384.7:c.1565del	ENSP00000419060.2:p.Lys522SerfsTer29
ENST00000497784.2:c.*1015del	ENSP00000420119.2:n.*1015del
ENST00000642228.1:c.*643del	ENSP00000493678.1:n.*643del
ENST00000642875.1:n.1129del
ENST00000644120.1:n.1955del
ENST00000644650.1:c.661del
ENST00000644905.1:n.1654del
ENST00000644969.2:c.1685del MANE Plus Clinical	ENSP00000496776.1:p.Lys562SerfsTer29
ENST00000646730.1:c.1565del	ENSP00000494784.1:p.Lys522SerfsTer29
ENST00000646891.1:c.1565del	ENSP00000493543.1:p.Lys522SerfsTer29
ENST00000647434.1:c.608del	ENSP00000495132.1:p.Lys203SerfsTer29
ENST00000288602.10:c.1565del	ENSP00000288602.6:p.Lys522SerfsTer29
ENST00000496384.6:c.388del
ENST00000497784.1:c.1600del	ENSP00000420119.1:n.1600del
NM_004333.4:c.1565del , LRG_299t1:c.1565del	NP_004324.2:p.Lys522SerfsTer29
XM_005250045.1:c.1565del	XP_005250102.1:p.Lys522SerfsTer29
XM_005250046.1:c.1565del	XP_005250103.1:p.Lys522SerfsTer29
XM_011516529.1:c.1565del	XP_011514831.1:p.Lys522SerfsTer29
XM_011516530.1:c.1565del	XP_011514832.1:p.Lys522SerfsTer29
XR_242190.1:n.1573del
XR_927520.1:n.1573del
XR_927521.1:n.1573del
XR_927522.1:n.1573del
XR_927523.1:n.1573del
NM_001354609.1:c.1565del	NP_001341538.1:p.Lys522SerfsTer29
NM_004333.5:c.1565del	NP_004324.2:p.Lys522SerfsTer29
NR_148928.1:n.1870del
XM_017012558.1:c.1685del	XP_016868047.1:p.Lys562SerfsTer29
XM_017012559.1:c.1685del	XP_016868048.1:p.Lys562SerfsTer29
XR_001744857.1:n.1693del
XR_001744858.1:n.1693del
NM_001354609.2:c.1565del	NP_001341538.1:p.Lys522SerfsTer29
NM_001374244.1:c.1685del	NP_001361173.1:p.Lys562SerfsTer29
NM_001374258.1:c.1685del MANE Plus Clinical	NP_001361187.1:p.Lys562SerfsTer29
NM_004333.6:c.1565del MANE Select	NP_004324.2:p.Lys522SerfsTer29
NM_001378467.1:c.1574del	NP_001365396.1:p.Lys525SerfsTer29
NM_001378468.1:c.1565del	NP_001365397.1:p.Lys522SerfsTer29
NM_001378469.1:c.1499del	NP_001365398.1:p.Lys500SerfsTer29
NM_001378470.1:c.1463del	NP_001365399.1:p.Lys488SerfsTer29
NM_001378471.1:c.1454del	NP_001365400.1:p.Lys485SerfsTer29
NM_001378472.1:c.1409del	NP_001365401.1:p.Lys470SerfsTer29
NM_001378473.1:c.1409del	NP_001365402.1:p.Lys470SerfsTer29
NM_001378474.1:c.1565del	NP_001365403.1:p.Lys522SerfsTer29
NM_001378475.1:c.1301del	NP_001365404.1:p.Lys434SerfsTer29