Canonical Allele Identifier: CA2518214444

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140801316_140801322del , CM000669.2:g.140801316_140801322del	GRCh38
NC_000007.13:g.140501116_140501122del , CM000669.1:g.140501116_140501122del	GRCh37
NC_000007.12:g.140147585_140147591del	NCBI36
NG_007873.3:g.128443_128449del , LRG_299:g.128443_128449del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.860+90_860+96del MANE Select	ENSP00000493543.1:n.860+90_860+96del
ENST00000288602.11:c.860+90_860+96del	ENSP00000288602.7:n.860+90_860+96del
ENST00000496384.7:c.860+90_860+96del	ENSP00000419060.2:n.860+90_860+96del
ENST00000497784.2:c.*310+90_*310+96del	ENSP00000420119.2:n.*310+90_*310+96del
ENST00000642228.1:c.860+90_860+96del	ENSP00000493678.1:n.860+90_860+96del
ENST00000642272.1:n.892+90_892+96del
ENST00000642875.1:n.354+90_354+96del
ENST00000643356.1:n.551_557del
ENST00000644120.1:n.1302+90_1302+96del
ENST00000644905.1:n.949+90_949+96del
ENST00000644969.2:c.860+90_860+96del MANE Plus Clinical	ENSP00000496776.1:n.860+90_860+96del
ENST00000646730.1:c.860+90_860+96del	ENSP00000494784.1:n.860+90_860+96del
ENST00000646891.1:c.860+90_860+96del	ENSP00000493543.1:n.860+90_860+96del
ENST00000288602.10:c.860+90_860+96del	ENSP00000288602.6:n.860+90_860+96del
ENST00000497784.1:c.895+90_895+96del	ENSP00000420119.1:n.895+90_895+96del
NM_004333.4:c.860+90_860+96del , LRG_299t1:c.860+90_860+96del	NP_004324.2:n.860+90_860+96del
XM_005250045.1:c.860+90_860+96del	XP_005250102.1:n.860+90_860+96del
XM_005250046.1:c.860+90_860+96del	XP_005250103.1:n.860+90_860+96del
XM_011516529.1:c.860+90_860+96del	XP_011514831.1:n.860+90_860+96del
XM_011516530.1:c.860+90_860+96del	XP_011514832.1:n.860+90_860+96del
XR_242190.1:n.868+90_868+96del
XR_927520.1:n.868+90_868+96del
XR_927521.1:n.868+90_868+96del
XR_927522.1:n.868+90_868+96del
XR_927523.1:n.868+90_868+96del
NM_001354609.1:c.860+90_860+96del	NP_001341538.1:n.860+90_860+96del
NM_004333.5:c.860+90_860+96del	NP_004324.2:n.860+90_860+96del
NR_148928.1:n.1165+90_1165+96del
XM_017012558.1:c.860+90_860+96del	XP_016868047.1:n.860+90_860+96del
XM_017012559.1:c.860+90_860+96del	XP_016868048.1:n.860+90_860+96del
XR_001744857.1:n.868+90_868+96del
XR_001744858.1:n.868+90_868+96del
NM_001354609.2:c.860+90_860+96del	NP_001341538.1:n.860+90_860+96del
NM_001374244.1:c.860+90_860+96del	NP_001361173.1:n.860+90_860+96del
NM_001374258.1:c.860+90_860+96del MANE Plus Clinical	NP_001361187.1:n.860+90_860+96del
NM_004333.6:c.860+90_860+96del MANE Select	NP_004324.2:n.860+90_860+96del
NM_001378467.1:c.869+90_869+96del	NP_001365396.1:n.869+90_869+96del
NM_001378468.1:c.860+90_860+96del	NP_001365397.1:n.860+90_860+96del
NM_001378469.1:c.860+90_860+96del	NP_001365398.1:n.860+90_860+96del
NM_001378470.1:c.758+90_758+96del	NP_001365399.1:n.758+90_758+96del
NM_001378471.1:c.860+90_860+96del	NP_001365400.1:n.860+90_860+96del
NM_001378472.1:c.704+90_704+96del	NP_001365401.1:n.704+90_704+96del
NM_001378473.1:c.704+90_704+96del	NP_001365402.1:n.704+90_704+96del
NM_001378474.1:c.860+90_860+96del	NP_001365403.1:n.860+90_860+96del
NM_001378475.1:c.596+90_596+96del	NP_001365404.1:n.596+90_596+96del