Canonical Allele Identifier: CA168047688

Gene: BRAF

Linked Data

• dbSNP Id: rs763738351
• gnomAD v3: 7-140753513-CAT-C
• gnomAD v4: 7-140753513-CAT-C
• MyVariant Identifiers: chr7:g.140453314_140453315del (hg19) ; chr7:g.140753514_140753515del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753515_140753516del , CM000669.2:g.140753515_140753516del	GRCh38
NC_000007.13:g.140453315_140453316del , CM000669.1:g.140453315_140453316del	GRCh37
NC_000007.12:g.140099784_140099785del	NCBI36
NG_007873.3:g.176250_176251del , LRG_299:g.176250_176251del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1742-122_1742-121del MANE Select	ENSP00000493543.1:n.1742-122_1742-121del
ENST00000288602.11:c.1862-122_1862-121del	ENSP00000288602.7:n.1862-122_1862-121del
ENST00000479537.6:c.412-122_412-121del
ENST00000496384.7:c.1742-122_1742-121del	ENSP00000419060.2:n.1742-122_1742-121del
ENST00000497784.2:c.*1192-122_*1192-121del	ENSP00000420119.2:n.*1192-122_*1192-121del
ENST00000642228.1:c.*820-122_*820-121del	ENSP00000493678.1:n.*820-122_*820-121del
ENST00000642875.1:n.1259-4097_1259-4096del
ENST00000644120.1:n.2132-122_2132-121del
ENST00000644650.1:c.838-122_838-121del
ENST00000644905.1:n.2502_2503del
ENST00000644969.2:c.1862-122_1862-121del MANE Plus Clinical	ENSP00000496776.1:n.1862-122_1862-121del
ENST00000646730.1:c.*318-122_*318-121del	ENSP00000494784.1:n.*318-122_*318-121del
ENST00000646891.1:c.1742-122_1742-121del	ENSP00000493543.1:n.1742-122_1742-121del
ENST00000647434.1:c.738-4097_738-4096del	ENSP00000495132.1:n.738-4097_738-4096del
ENST00000288602.10:c.1742-122_1742-121del	ENSP00000288602.6:n.1742-122_1742-121del
ENST00000479537.5:c.26-122_26-121del	ENSP00000418033.1:n.26-122_26-121del
ENST00000496384.6:c.565-122_565-121del
ENST00000497784.1:c.1777-122_1777-121del	ENSP00000420119.1:n.1777-122_1777-121del
NM_004333.4:c.1742-122_1742-121del , LRG_299t1:c.1742-122_1742-121del	NP_004324.2:n.1742-122_1742-121del
XM_005250045.1:c.1742-122_1742-121del	XP_005250102.1:n.1742-122_1742-121del
XM_005250046.1:c.1742-122_1742-121del	XP_005250103.1:n.1742-122_1742-121del
XM_011516529.1:c.1742-122_1742-121del	XP_011514831.1:n.1742-122_1742-121del
XM_011516530.1:c.1695-4097_1695-4096del	XP_011514832.1:n.1695-4097_1695-4096del
XR_242190.1:n.1750-122_1750-121del
XR_927520.1:n.1750-122_1750-121del
XR_927521.1:n.1750-122_1750-121del
XR_927522.1:n.1703-4097_1703-4096del
XR_927523.1:n.1703-4097_1703-4096del
NM_001354609.1:c.1742-122_1742-121del	NP_001341538.1:n.1742-122_1742-121del
NM_004333.5:c.1742-122_1742-121del	NP_004324.2:n.1742-122_1742-121del
NR_148928.1:n.2718_2719del
XM_017012558.1:c.1862-122_1862-121del	XP_016868047.1:n.1862-122_1862-121del
XM_017012559.1:c.1862-122_1862-121del	XP_016868048.1:n.1862-122_1862-121del
XR_001744857.1:n.1870-122_1870-121del
XR_001744858.1:n.1823-4097_1823-4096del
NM_001354609.2:c.1742-122_1742-121del	NP_001341538.1:n.1742-122_1742-121del
NM_001374244.1:c.1862-122_1862-121del	NP_001361173.1:n.1862-122_1862-121del
NM_001374258.1:c.1862-122_1862-121del MANE Plus Clinical	NP_001361187.1:n.1862-122_1862-121del
NM_004333.6:c.1742-122_1742-121del MANE Select	NP_004324.2:n.1742-122_1742-121del
NM_001378467.1:c.1751-122_1751-121del	NP_001365396.1:n.1751-122_1751-121del
NM_001378468.1:c.1742-122_1742-121del	NP_001365397.1:n.1742-122_1742-121del
NM_001378469.1:c.1676-122_1676-121del	NP_001365398.1:n.1676-122_1676-121del
NM_001378470.1:c.1640-122_1640-121del	NP_001365399.1:n.1640-122_1640-121del
NM_001378471.1:c.1631-122_1631-121del	NP_001365400.1:n.1631-122_1631-121del
NM_001378472.1:c.1586-122_1586-121del	NP_001365401.1:n.1586-122_1586-121del
NM_001378473.1:c.1586-122_1586-121del	NP_001365402.1:n.1586-122_1586-121del
NM_001378474.1:c.1742-122_1742-121del	NP_001365403.1:n.1742-122_1742-121del
NM_001378475.1:c.1478-122_1478-121del	NP_001365404.1:n.1478-122_1478-121del