Canonical Allele Identifier: CA2685242134

Gene: BRAF

Linked Data

• gnomAD v4: 7-140781398-AAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140781400_140781401del , CM000669.2:g.140781400_140781401del	GRCh38
NC_000007.13:g.140481200_140481201del , CM000669.1:g.140481200_140481201del	GRCh37
NC_000007.12:g.140127669_140127670del	NCBI36
NG_007873.3:g.148365_148366del , LRG_299:g.148365_148366del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1432+176_1432+177del MANE Select	ENSP00000493543.1:n.1432+176_1432+177del
ENST00000288602.11:c.1552+176_1552+177del	ENSP00000288602.7:n.1552+176_1552+177del
ENST00000479537.6:c.102+176_102+177del
ENST00000496384.7:c.1432+176_1432+177del	ENSP00000419060.2:n.1432+176_1432+177del
ENST00000497784.2:c.*882+176_*882+177del	ENSP00000420119.2:n.*882+176_*882+177del
ENST00000642228.1:c.*510+176_*510+177del	ENSP00000493678.1:n.*510+176_*510+177del
ENST00000642875.1:n.874+176_874+177del
ENST00000644120.1:n.1822+176_1822+177del
ENST00000644650.1:c.528+176_528+177del
ENST00000644905.1:n.1521+176_1521+177del
ENST00000644969.2:c.1552+176_1552+177del MANE Plus Clinical	ENSP00000496776.1:n.1552+176_1552+177del
ENST00000646334.1:n.738_739del
ENST00000646730.1:c.1432+176_1432+177del	ENSP00000494784.1:n.1432+176_1432+177del
ENST00000646891.1:c.1432+176_1432+177del	ENSP00000493543.1:n.1432+176_1432+177del
ENST00000647434.1:c.475+176_475+177del	ENSP00000495132.1:n.475+176_475+177del
ENST00000288602.10:c.1432+176_1432+177del	ENSP00000288602.6:n.1432+176_1432+177del
ENST00000496384.6:c.255+176_255+177del
ENST00000497784.1:c.1467+176_1467+177del	ENSP00000420119.1:n.1467+176_1467+177del
NM_004333.4:c.1432+176_1432+177del , LRG_299t1:c.1432+176_1432+177del	NP_004324.2:n.1432+176_1432+177del
XM_005250045.1:c.1432+176_1432+177del	XP_005250102.1:n.1432+176_1432+177del
XM_005250046.1:c.1432+176_1432+177del	XP_005250103.1:n.1432+176_1432+177del
XM_011516529.1:c.1432+176_1432+177del	XP_011514831.1:n.1432+176_1432+177del
XM_011516530.1:c.1432+176_1432+177del	XP_011514832.1:n.1432+176_1432+177del
XR_242190.1:n.1440+176_1440+177del
XR_927520.1:n.1440+176_1440+177del
XR_927521.1:n.1440+176_1440+177del
XR_927522.1:n.1440+176_1440+177del
XR_927523.1:n.1440+176_1440+177del
NM_001354609.1:c.1432+176_1432+177del	NP_001341538.1:n.1432+176_1432+177del
NM_004333.5:c.1432+176_1432+177del	NP_004324.2:n.1432+176_1432+177del
NR_148928.1:n.1737+176_1737+177del
XM_017012558.1:c.1552+176_1552+177del	XP_016868047.1:n.1552+176_1552+177del
XM_017012559.1:c.1552+176_1552+177del	XP_016868048.1:n.1552+176_1552+177del
XR_001744857.1:n.1560+176_1560+177del
XR_001744858.1:n.1560+176_1560+177del
NM_001354609.2:c.1432+176_1432+177del	NP_001341538.1:n.1432+176_1432+177del
NM_001374244.1:c.1552+176_1552+177del	NP_001361173.1:n.1552+176_1552+177del
NM_001374258.1:c.1552+176_1552+177del MANE Plus Clinical	NP_001361187.1:n.1552+176_1552+177del
NM_004333.6:c.1432+176_1432+177del MANE Select	NP_004324.2:n.1432+176_1432+177del
NM_001378467.1:c.1441+176_1441+177del	NP_001365396.1:n.1441+176_1441+177del
NM_001378468.1:c.1432+176_1432+177del	NP_001365397.1:n.1432+176_1432+177del
NM_001378469.1:c.1366+176_1366+177del	NP_001365398.1:n.1366+176_1366+177del
NM_001378470.1:c.1330+176_1330+177del	NP_001365399.1:n.1330+176_1330+177del
NM_001378471.1:c.1321+176_1321+177del	NP_001365400.1:n.1321+176_1321+177del
NM_001378472.1:c.1276+176_1276+177del	NP_001365401.1:n.1276+176_1276+177del
NM_001378473.1:c.1276+176_1276+177del	NP_001365402.1:n.1276+176_1276+177del
NM_001378474.1:c.1432+176_1432+177del	NP_001365403.1:n.1432+176_1432+177del
NM_001378475.1:c.1168+176_1168+177del	NP_001365404.1:n.1168+176_1168+177del