Canonical Allele Identifier: CA578269172

Gene: BRAF

Linked Data

• dbSNP Id: rs1562941574
• gnomAD v2: 7-140453940-AAGTC-A
• gnomAD v4: 7-140754140-AAGTC-A
• MyVariant Identifiers: chr7:g.140453941_140453944del (hg19) ; chr7:g.140754141_140754144del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140754143_140754146del , CM000669.2:g.140754143_140754146del	GRCh38
NC_000007.13:g.140453943_140453946del , CM000669.1:g.140453943_140453946del	GRCh37
NC_000007.12:g.140100412_140100415del	NCBI36
NG_007873.3:g.175621_175624del , LRG_299:g.175621_175624del

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1741+43_1741+46del MANE Select	ENSP00000493543.1:n.1741+43_1741+46del
ENST00000288602.11:c.1861+43_1861+46del	ENSP00000288602.7:n.1861+43_1861+46del
ENST00000479537.6:c.411+43_411+46del
ENST00000496384.7:c.1741+43_1741+46del	ENSP00000419060.2:n.1741+43_1741+46del
ENST00000497784.2:c.*1191+43_*1191+46del	ENSP00000420119.2:n.*1191+43_*1191+46del
ENST00000642228.1:c.*819+43_*819+46del	ENSP00000493678.1:n.*819+43_*819+46del
ENST00000642875.1:n.1259-4726_1259-4723del
ENST00000644120.1:n.2131+43_2131+46del
ENST00000644650.1:c.837+43_837+46del
ENST00000644905.1:n.1873_1876del
ENST00000644969.2:c.1861+43_1861+46del MANE Plus Clinical	ENSP00000496776.1:n.1861+43_1861+46del
ENST00000646730.1:c.*317+43_*317+46del	ENSP00000494784.1:n.*317+43_*317+46del
ENST00000646891.1:c.1741+43_1741+46del	ENSP00000493543.1:n.1741+43_1741+46del
ENST00000647434.1:c.738-4726_738-4723del	ENSP00000495132.1:n.738-4726_738-4723del
ENST00000288602.10:c.1741+43_1741+46del	ENSP00000288602.6:n.1741+43_1741+46del
ENST00000479537.5:c.25+43_25+46del	ENSP00000418033.1:n.25+43_25+46del
ENST00000496384.6:c.564+43_564+46del
ENST00000497784.1:c.1776+43_1776+46del	ENSP00000420119.1:n.1776+43_1776+46del
NM_004333.4:c.1741+43_1741+46del , LRG_299t1:c.1741+43_1741+46del	NP_004324.2:n.1741+43_1741+46del
XM_005250045.1:c.1741+43_1741+46del	XP_005250102.1:n.1741+43_1741+46del
XM_005250046.1:c.1741+43_1741+46del	XP_005250103.1:n.1741+43_1741+46del
XM_011516529.1:c.1741+43_1741+46del	XP_011514831.1:n.1741+43_1741+46del
XM_011516530.1:c.1695-4726_1695-4723del	XP_011514832.1:n.1695-4726_1695-4723del
XR_242190.1:n.1749+43_1749+46del
XR_927520.1:n.1749+43_1749+46del
XR_927521.1:n.1749+43_1749+46del
XR_927522.1:n.1703-4726_1703-4723del
XR_927523.1:n.1703-4726_1703-4723del
NM_001354609.1:c.1741+43_1741+46del	NP_001341538.1:n.1741+43_1741+46del
NM_004333.5:c.1741+43_1741+46del	NP_004324.2:n.1741+43_1741+46del
NR_148928.1:n.2089_2092del
XM_017012558.1:c.1861+43_1861+46del	XP_016868047.1:n.1861+43_1861+46del
XM_017012559.1:c.1861+43_1861+46del	XP_016868048.1:n.1861+43_1861+46del
XR_001744857.1:n.1869+43_1869+46del
XR_001744858.1:n.1823-4726_1823-4723del
NM_001354609.2:c.1741+43_1741+46del	NP_001341538.1:n.1741+43_1741+46del
NM_001374244.1:c.1861+43_1861+46del	NP_001361173.1:n.1861+43_1861+46del
NM_001374258.1:c.1861+43_1861+46del MANE Plus Clinical	NP_001361187.1:n.1861+43_1861+46del
NM_004333.6:c.1741+43_1741+46del MANE Select	NP_004324.2:n.1741+43_1741+46del
NM_001378467.1:c.1750+43_1750+46del	NP_001365396.1:n.1750+43_1750+46del
NM_001378468.1:c.1741+43_1741+46del	NP_001365397.1:n.1741+43_1741+46del
NM_001378469.1:c.1675+43_1675+46del	NP_001365398.1:n.1675+43_1675+46del
NM_001378470.1:c.1639+43_1639+46del	NP_001365399.1:n.1639+43_1639+46del
NM_001378471.1:c.1630+43_1630+46del	NP_001365400.1:n.1630+43_1630+46del
NM_001378472.1:c.1585+43_1585+46del	NP_001365401.1:n.1585+43_1585+46del
NM_001378473.1:c.1585+43_1585+46del	NP_001365402.1:n.1585+43_1585+46del
NM_001378474.1:c.1741+43_1741+46del	NP_001365403.1:n.1741+43_1741+46del
NM_001378475.1:c.1477+43_1477+46del	NP_001365404.1:n.1477+43_1477+46del