Canonical Allele Identifier: CA2579043660

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140777008_140777009insGGCCT , CM000669.2:g.140777008_140777009insGGCCT	GRCh38
NC_000007.13:g.140476808_140476809insGGCCT , CM000669.1:g.140476808_140476809insGGCCT	GRCh37
NC_000007.12:g.140123277_140123278insGGCCT	NCBI36
NG_007873.3:g.152759_152760insCCAGG , LRG_299:g.152759_152760insCCAGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1600_1601insCCAGG MANE Select	ENSP00000493543.1:p.Gly534AlafsTer19
ENST00000288602.11:c.1720_1721insCCAGG	ENSP00000288602.7:p.Gly574AlafsTer19
ENST00000479537.6:c.270_271insCCAGG
ENST00000496384.7:c.1600_1601insCCAGG	ENSP00000419060.2:p.Gly534AlafsTer19
ENST00000497784.2:c.*1050_*1051insCCAGG	ENSP00000420119.2:n.*1050_*1051insCCAGG
ENST00000642228.1:c.*678_*679insCCAGG	ENSP00000493678.1:n.*678_*679insCCAGG
ENST00000642875.1:n.1164_1165insCCAGG
ENST00000644120.1:n.1990_1991insCCAGG
ENST00000644650.1:c.696_697insCCAGG
ENST00000644905.1:n.1689_1690insCCAGG
ENST00000644969.2:c.1720_1721insCCAGG MANE Plus Clinical	ENSP00000496776.1:p.Gly574AlafsTer19
ENST00000646730.1:c.1600_1601insCCAGG	ENSP00000494784.1:p.Gly534AlafsTer19
ENST00000646891.1:c.1600_1601insCCAGG	ENSP00000493543.1:p.Gly534AlafsTer19
ENST00000647434.1:c.643_644insCCAGG	ENSP00000495132.1:p.Gly215AlafsTer19
ENST00000288602.10:c.1600_1601insCCAGG	ENSP00000288602.6:p.Gly534AlafsTer19
ENST00000496384.6:c.423_424insCCAGG
ENST00000497784.1:c.1635_1636insCCAGG	ENSP00000420119.1:n.1635_1636insCCAGG
NM_004333.4:c.1600_1601insCCAGG , LRG_299t1:c.1600_1601insCCAGG	NP_004324.2:p.Gly534AlafsTer19
XM_005250045.1:c.1600_1601insCCAGG	XP_005250102.1:p.Gly534AlafsTer19
XM_005250046.1:c.1600_1601insCCAGG	XP_005250103.1:p.Gly534AlafsTer19
XM_011516529.1:c.1600_1601insCCAGG	XP_011514831.1:p.Gly534AlafsTer19
XM_011516530.1:c.1600_1601insCCAGG	XP_011514832.1:p.Gly534AlafsTer19
XR_242190.1:n.1608_1609insCCAGG
XR_927520.1:n.1608_1609insCCAGG
XR_927521.1:n.1608_1609insCCAGG
XR_927522.1:n.1608_1609insCCAGG
XR_927523.1:n.1608_1609insCCAGG
NM_001354609.1:c.1600_1601insCCAGG	NP_001341538.1:p.Gly534AlafsTer19
NM_004333.5:c.1600_1601insCCAGG	NP_004324.2:p.Gly534AlafsTer19
NR_148928.1:n.1905_1906insCCAGG
XM_017012558.1:c.1720_1721insCCAGG	XP_016868047.1:p.Gly574AlafsTer19
XM_017012559.1:c.1720_1721insCCAGG	XP_016868048.1:p.Gly574AlafsTer19
XR_001744857.1:n.1728_1729insCCAGG
XR_001744858.1:n.1728_1729insCCAGG
NM_001354609.2:c.1600_1601insCCAGG	NP_001341538.1:p.Gly534AlafsTer19
NM_001374244.1:c.1720_1721insCCAGG	NP_001361173.1:p.Gly574AlafsTer19
NM_001374258.1:c.1720_1721insCCAGG MANE Plus Clinical	NP_001361187.1:p.Gly574AlafsTer19
NM_004333.6:c.1600_1601insCCAGG MANE Select	NP_004324.2:p.Gly534AlafsTer19
NM_001378467.1:c.1609_1610insCCAGG	NP_001365396.1:p.Gly537AlafsTer19
NM_001378468.1:c.1600_1601insCCAGG	NP_001365397.1:p.Gly534AlafsTer19
NM_001378469.1:c.1534_1535insCCAGG	NP_001365398.1:p.Gly512AlafsTer19
NM_001378470.1:c.1498_1499insCCAGG	NP_001365399.1:p.Gly500AlafsTer19
NM_001378471.1:c.1489_1490insCCAGG	NP_001365400.1:p.Gly497AlafsTer19
NM_001378472.1:c.1444_1445insCCAGG	NP_001365401.1:p.Gly482AlafsTer19
NM_001378473.1:c.1444_1445insCCAGG	NP_001365402.1:p.Gly482AlafsTer19
NM_001378474.1:c.1600_1601insCCAGG	NP_001365403.1:p.Gly534AlafsTer19
NM_001378475.1:c.1336_1337insCCAGG	NP_001365404.1:p.Gly446AlafsTer19