Canonical Allele Identifier: CA2685224279

Gene: BRAF

Linked Data

• gnomAD v4: 7-140754014-AAGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140754017_140754019del , CM000669.2:g.140754017_140754019del	GRCh38
NC_000007.13:g.140453817_140453819del , CM000669.1:g.140453817_140453819del	GRCh37
NC_000007.12:g.140100286_140100288del	NCBI36
NG_007873.3:g.175748_175750del , LRG_299:g.175748_175750del

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1741+170_1741+172del MANE Select	ENSP00000493543.1:n.1741+170_1741+172del
ENST00000288602.11:c.1861+170_1861+172del	ENSP00000288602.7:n.1861+170_1861+172del
ENST00000479537.6:c.411+170_411+172del
ENST00000496384.7:c.1741+170_1741+172del	ENSP00000419060.2:n.1741+170_1741+172del
ENST00000497784.2:c.*1191+170_*1191+172del	ENSP00000420119.2:n.*1191+170_*1191+172de...
ENST00000642228.1:c.*819+170_*819+172del	ENSP00000493678.1:n.*819+170_*819+172del
ENST00000642875.1:n.1259-4599_1259-4597del
ENST00000644120.1:n.2131+170_2131+172del
ENST00000644650.1:c.837+170_837+172del
ENST00000644905.1:n.2000_2002del
ENST00000644969.2:c.1861+170_1861+172del MANE Plus Clinical	ENSP00000496776.1:n.1861+170_1861+172del
ENST00000646730.1:c.*317+170_*317+172del	ENSP00000494784.1:n.*317+170_*317+172del
ENST00000646891.1:c.1741+170_1741+172del	ENSP00000493543.1:n.1741+170_1741+172del
ENST00000647434.1:c.738-4599_738-4597del	ENSP00000495132.1:n.738-4599_738-4597del
ENST00000288602.10:c.1741+170_1741+172del	ENSP00000288602.6:n.1741+170_1741+172del
ENST00000479537.5:c.25+170_25+172del	ENSP00000418033.1:n.25+170_25+172del
ENST00000496384.6:c.564+170_564+172del
ENST00000497784.1:c.1776+170_1776+172del	ENSP00000420119.1:n.1776+170_1776+172del
NM_004333.4:c.1741+170_1741+172del , LRG_299t1:c.1741+170_1741+172del	NP_004324.2:n.1741+170_1741+172del
XM_005250045.1:c.1741+170_1741+172del	XP_005250102.1:n.1741+170_1741+172del
XM_005250046.1:c.1741+170_1741+172del	XP_005250103.1:n.1741+170_1741+172del
XM_011516529.1:c.1741+170_1741+172del	XP_011514831.1:n.1741+170_1741+172del
XM_011516530.1:c.1695-4599_1695-4597del	XP_011514832.1:n.1695-4599_1695-4597del
XR_242190.1:n.1749+170_1749+172del
XR_927520.1:n.1749+170_1749+172del
XR_927521.1:n.1749+170_1749+172del
XR_927522.1:n.1703-4599_1703-4597del
XR_927523.1:n.1703-4599_1703-4597del
NM_001354609.1:c.1741+170_1741+172del	NP_001341538.1:n.1741+170_1741+172del
NM_004333.5:c.1741+170_1741+172del	NP_004324.2:n.1741+170_1741+172del
NR_148928.1:n.2216_2218del
XM_017012558.1:c.1861+170_1861+172del	XP_016868047.1:n.1861+170_1861+172del
XM_017012559.1:c.1861+170_1861+172del	XP_016868048.1:n.1861+170_1861+172del
XR_001744857.1:n.1869+170_1869+172del
XR_001744858.1:n.1823-4599_1823-4597del
NM_001354609.2:c.1741+170_1741+172del	NP_001341538.1:n.1741+170_1741+172del
NM_001374244.1:c.1861+170_1861+172del	NP_001361173.1:n.1861+170_1861+172del
NM_001374258.1:c.1861+170_1861+172del MANE Plus Clinical	NP_001361187.1:n.1861+170_1861+172del
NM_004333.6:c.1741+170_1741+172del MANE Select	NP_004324.2:n.1741+170_1741+172del
NM_001378467.1:c.1750+170_1750+172del	NP_001365396.1:n.1750+170_1750+172del
NM_001378468.1:c.1741+170_1741+172del	NP_001365397.1:n.1741+170_1741+172del
NM_001378469.1:c.1675+170_1675+172del	NP_001365398.1:n.1675+170_1675+172del
NM_001378470.1:c.1639+170_1639+172del	NP_001365399.1:n.1639+170_1639+172del
NM_001378471.1:c.1630+170_1630+172del	NP_001365400.1:n.1630+170_1630+172del
NM_001378472.1:c.1585+170_1585+172del	NP_001365401.1:n.1585+170_1585+172del
NM_001378473.1:c.1585+170_1585+172del	NP_001365402.1:n.1585+170_1585+172del
NM_001378474.1:c.1741+170_1741+172del	NP_001365403.1:n.1741+170_1741+172del
NM_001378475.1:c.1477+170_1477+172del	NP_001365404.1:n.1477+170_1477+172del