Canonical Allele Identifier: CA2685242138

Gene: BRAF

Linked Data

• gnomAD v4: 7-140781402-GTTTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140781404_140781407del , CM000669.2:g.140781404_140781407del	GRCh38
NC_000007.13:g.140481204_140481207del , CM000669.1:g.140481204_140481207del	GRCh37
NC_000007.12:g.140127673_140127676del	NCBI36
NG_007873.3:g.148359_148362del , LRG_299:g.148359_148362del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1432+170_1432+173del MANE Select	ENSP00000493543.1:n.1432+170_1432+173del
ENST00000288602.11:c.1552+170_1552+173del	ENSP00000288602.7:n.1552+170_1552+173del
ENST00000479537.6:c.102+170_102+173del
ENST00000496384.7:c.1432+170_1432+173del	ENSP00000419060.2:n.1432+170_1432+173del
ENST00000497784.2:c.*882+170_*882+173del	ENSP00000420119.2:n.*882+170_*882+173del
ENST00000642228.1:c.*510+170_*510+173del	ENSP00000493678.1:n.*510+170_*510+173del
ENST00000642875.1:n.874+170_874+173del
ENST00000644120.1:n.1822+170_1822+173del
ENST00000644650.1:c.528+170_528+173del
ENST00000644905.1:n.1521+170_1521+173del
ENST00000644969.2:c.1552+170_1552+173del MANE Plus Clinical	ENSP00000496776.1:n.1552+170_1552+173del
ENST00000646334.1:n.732_735del
ENST00000646730.1:c.1432+170_1432+173del	ENSP00000494784.1:n.1432+170_1432+173del
ENST00000646891.1:c.1432+170_1432+173del	ENSP00000493543.1:n.1432+170_1432+173del
ENST00000647434.1:c.475+170_475+173del	ENSP00000495132.1:n.475+170_475+173del
ENST00000288602.10:c.1432+170_1432+173del	ENSP00000288602.6:n.1432+170_1432+173del
ENST00000496384.6:c.255+170_255+173del
ENST00000497784.1:c.1467+170_1467+173del	ENSP00000420119.1:n.1467+170_1467+173del
NM_004333.4:c.1432+170_1432+173del , LRG_299t1:c.1432+170_1432+173del	NP_004324.2:n.1432+170_1432+173del
XM_005250045.1:c.1432+170_1432+173del	XP_005250102.1:n.1432+170_1432+173del
XM_005250046.1:c.1432+170_1432+173del	XP_005250103.1:n.1432+170_1432+173del
XM_011516529.1:c.1432+170_1432+173del	XP_011514831.1:n.1432+170_1432+173del
XM_011516530.1:c.1432+170_1432+173del	XP_011514832.1:n.1432+170_1432+173del
XR_242190.1:n.1440+170_1440+173del
XR_927520.1:n.1440+170_1440+173del
XR_927521.1:n.1440+170_1440+173del
XR_927522.1:n.1440+170_1440+173del
XR_927523.1:n.1440+170_1440+173del
NM_001354609.1:c.1432+170_1432+173del	NP_001341538.1:n.1432+170_1432+173del
NM_004333.5:c.1432+170_1432+173del	NP_004324.2:n.1432+170_1432+173del
NR_148928.1:n.1737+170_1737+173del
XM_017012558.1:c.1552+170_1552+173del	XP_016868047.1:n.1552+170_1552+173del
XM_017012559.1:c.1552+170_1552+173del	XP_016868048.1:n.1552+170_1552+173del
XR_001744857.1:n.1560+170_1560+173del
XR_001744858.1:n.1560+170_1560+173del
NM_001354609.2:c.1432+170_1432+173del	NP_001341538.1:n.1432+170_1432+173del
NM_001374244.1:c.1552+170_1552+173del	NP_001361173.1:n.1552+170_1552+173del
NM_001374258.1:c.1552+170_1552+173del MANE Plus Clinical	NP_001361187.1:n.1552+170_1552+173del
NM_004333.6:c.1432+170_1432+173del MANE Select	NP_004324.2:n.1432+170_1432+173del
NM_001378467.1:c.1441+170_1441+173del	NP_001365396.1:n.1441+170_1441+173del
NM_001378468.1:c.1432+170_1432+173del	NP_001365397.1:n.1432+170_1432+173del
NM_001378469.1:c.1366+170_1366+173del	NP_001365398.1:n.1366+170_1366+173del
NM_001378470.1:c.1330+170_1330+173del	NP_001365399.1:n.1330+170_1330+173del
NM_001378471.1:c.1321+170_1321+173del	NP_001365400.1:n.1321+170_1321+173del
NM_001378472.1:c.1276+170_1276+173del	NP_001365401.1:n.1276+170_1276+173del
NM_001378473.1:c.1276+170_1276+173del	NP_001365402.1:n.1276+170_1276+173del
NM_001378474.1:c.1432+170_1432+173del	NP_001365403.1:n.1432+170_1432+173del
NM_001378475.1:c.1168+170_1168+173del	NP_001365404.1:n.1168+170_1168+173del