Canonical Allele Identifier: CA2685244094

Gene: BRAF

Linked Data

• gnomAD v4: 7-140800546-ATAGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140800549_140800552del , CM000669.2:g.140800549_140800552del	GRCh38
NC_000007.13:g.140500349_140500352del , CM000669.1:g.140500349_140500352del	GRCh37
NC_000007.12:g.140146818_140146821del	NCBI36
NG_007873.3:g.129215_129218del , LRG_299:g.129215_129218del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.861-69_861-66del MANE Select	ENSP00000493543.1:n.861-69_861-66del
ENST00000288602.11:c.861-69_861-66del	ENSP00000288602.7:n.861-69_861-66del
ENST00000496384.7:c.861-69_861-66del	ENSP00000419060.2:n.861-69_861-66del
ENST00000497784.2:c.*311-69_*311-66del	ENSP00000420119.2:n.*311-69_*311-66del
ENST00000642228.1:c.861-88_861-85del	ENSP00000493678.1:n.861-88_861-85del
ENST00000642272.1:n.893-69_893-66del
ENST00000642875.1:n.355-69_355-66del
ENST00000644120.1:n.1303-69_1303-66del
ENST00000644905.1:n.950-69_950-66del
ENST00000644969.2:c.861-69_861-66del MANE Plus Clinical	ENSP00000496776.1:n.861-69_861-66del
ENST00000646730.1:c.861-69_861-66del	ENSP00000494784.1:n.861-69_861-66del
ENST00000646891.1:c.861-69_861-66del	ENSP00000493543.1:n.861-69_861-66del
ENST00000288602.10:c.861-69_861-66del	ENSP00000288602.6:n.861-69_861-66del
ENST00000497784.1:c.896-69_896-66del	ENSP00000420119.1:n.896-69_896-66del
NM_004333.4:c.861-69_861-66del , LRG_299t1:c.861-69_861-66del	NP_004324.2:n.861-69_861-66del
XM_005250045.1:c.861-69_861-66del	XP_005250102.1:n.861-69_861-66del
XM_005250046.1:c.861-69_861-66del	XP_005250103.1:n.861-69_861-66del
XM_011516529.1:c.861-69_861-66del	XP_011514831.1:n.861-69_861-66del
XM_011516530.1:c.861-69_861-66del	XP_011514832.1:n.861-69_861-66del
XR_242190.1:n.869-69_869-66del
XR_927520.1:n.869-69_869-66del
XR_927521.1:n.869-69_869-66del
XR_927522.1:n.869-69_869-66del
XR_927523.1:n.869-69_869-66del
NM_001354609.1:c.861-69_861-66del	NP_001341538.1:n.861-69_861-66del
NM_004333.5:c.861-69_861-66del	NP_004324.2:n.861-69_861-66del
NR_148928.1:n.1166-69_1166-66del
XM_017012558.1:c.861-69_861-66del	XP_016868047.1:n.861-69_861-66del
XM_017012559.1:c.861-69_861-66del	XP_016868048.1:n.861-69_861-66del
XR_001744857.1:n.869-69_869-66del
XR_001744858.1:n.869-69_869-66del
NM_001354609.2:c.861-69_861-66del	NP_001341538.1:n.861-69_861-66del
NM_001374244.1:c.861-69_861-66del	NP_001361173.1:n.861-69_861-66del
NM_001374258.1:c.861-69_861-66del MANE Plus Clinical	NP_001361187.1:n.861-69_861-66del
NM_004333.6:c.861-69_861-66del MANE Select	NP_004324.2:n.861-69_861-66del
NM_001378467.1:c.870-69_870-66del	NP_001365396.1:n.870-69_870-66del
NM_001378468.1:c.861-69_861-66del	NP_001365397.1:n.861-69_861-66del
NM_001378469.1:c.861-69_861-66del	NP_001365398.1:n.861-69_861-66del
NM_001378470.1:c.759-69_759-66del	NP_001365399.1:n.759-69_759-66del
NM_001378471.1:c.861-69_861-66del	NP_001365400.1:n.861-69_861-66del
NM_001378472.1:c.705-69_705-66del	NP_001365401.1:n.705-69_705-66del
NM_001378473.1:c.705-69_705-66del	NP_001365402.1:n.705-69_705-66del
NM_001378474.1:c.861-69_861-66del	NP_001365403.1:n.861-69_861-66del
NM_001378475.1:c.597-69_597-66del	NP_001365404.1:n.597-69_597-66del