Canonical Allele Identifier: CA2685224018

Gene: BRAF

Linked Data

• gnomAD v4: 7-140753453-ATGAAGAGTTTAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753454_140753465del , CM000669.2:g.140753454_140753465del	GRCh38
NC_000007.13:g.140453254_140453265del , CM000669.1:g.140453254_140453265del	GRCh37
NC_000007.12:g.140099723_140099734del	NCBI36
NG_007873.3:g.176300_176311del , LRG_299:g.176300_176311del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1742-72_1742-61del MANE Select	ENSP00000493543.1:n.1742-72_1742-61del
ENST00000288602.11:c.1862-72_1862-61del	ENSP00000288602.7:n.1862-72_1862-61del
ENST00000479537.6:c.412-72_412-61del
ENST00000496384.7:c.1742-72_1742-61del	ENSP00000419060.2:n.1742-72_1742-61del
ENST00000497784.2:c.*1192-72_*1192-61del	ENSP00000420119.2:n.*1192-72_*1192-61del
ENST00000642228.1:c.*820-72_*820-61del	ENSP00000493678.1:n.*820-72_*820-61del
ENST00000642875.1:n.1259-4047_1259-4036del
ENST00000644120.1:n.2132-72_2132-61del
ENST00000644650.1:c.838-72_838-61del
ENST00000644905.1:n.2552_2563del
ENST00000644969.2:c.1862-72_1862-61del MANE Plus Clinical	ENSP00000496776.1:n.1862-72_1862-61del
ENST00000646730.1:c.*318-72_*318-61del	ENSP00000494784.1:n.*318-72_*318-61del
ENST00000646891.1:c.1742-72_1742-61del	ENSP00000493543.1:n.1742-72_1742-61del
ENST00000647434.1:c.738-4047_738-4036del	ENSP00000495132.1:n.738-4047_738-4036del
ENST00000288602.10:c.1742-72_1742-61del	ENSP00000288602.6:n.1742-72_1742-61del
ENST00000479537.5:c.26-72_26-61del	ENSP00000418033.1:n.26-72_26-61del
ENST00000496384.6:c.565-72_565-61del
ENST00000497784.1:c.1777-72_1777-61del	ENSP00000420119.1:n.1777-72_1777-61del
NM_004333.4:c.1742-72_1742-61del , LRG_299t1:c.1742-72_1742-61del	NP_004324.2:n.1742-72_1742-61del
XM_005250045.1:c.1742-72_1742-61del	XP_005250102.1:n.1742-72_1742-61del
XM_005250046.1:c.1742-72_1742-61del	XP_005250103.1:n.1742-72_1742-61del
XM_011516529.1:c.1742-72_1742-61del	XP_011514831.1:n.1742-72_1742-61del
XM_011516530.1:c.1695-4047_1695-4036del	XP_011514832.1:n.1695-4047_1695-4036del
XR_242190.1:n.1750-72_1750-61del
XR_927520.1:n.1750-72_1750-61del
XR_927521.1:n.1750-72_1750-61del
XR_927522.1:n.1703-4047_1703-4036del
XR_927523.1:n.1703-4047_1703-4036del
NM_001354609.1:c.1742-72_1742-61del	NP_001341538.1:n.1742-72_1742-61del
NM_004333.5:c.1742-72_1742-61del	NP_004324.2:n.1742-72_1742-61del
NR_148928.1:n.2768_2779del
XM_017012558.1:c.1862-72_1862-61del	XP_016868047.1:n.1862-72_1862-61del
XM_017012559.1:c.1862-72_1862-61del	XP_016868048.1:n.1862-72_1862-61del
XR_001744857.1:n.1870-72_1870-61del
XR_001744858.1:n.1823-4047_1823-4036del
NM_001354609.2:c.1742-72_1742-61del	NP_001341538.1:n.1742-72_1742-61del
NM_001374244.1:c.1862-72_1862-61del	NP_001361173.1:n.1862-72_1862-61del
NM_001374258.1:c.1862-72_1862-61del MANE Plus Clinical	NP_001361187.1:n.1862-72_1862-61del
NM_004333.6:c.1742-72_1742-61del MANE Select	NP_004324.2:n.1742-72_1742-61del
NM_001378467.1:c.1751-72_1751-61del	NP_001365396.1:n.1751-72_1751-61del
NM_001378468.1:c.1742-72_1742-61del	NP_001365397.1:n.1742-72_1742-61del
NM_001378469.1:c.1676-72_1676-61del	NP_001365398.1:n.1676-72_1676-61del
NM_001378470.1:c.1640-72_1640-61del	NP_001365399.1:n.1640-72_1640-61del
NM_001378471.1:c.1631-72_1631-61del	NP_001365400.1:n.1631-72_1631-61del
NM_001378472.1:c.1586-72_1586-61del	NP_001365401.1:n.1586-72_1586-61del
NM_001378473.1:c.1586-72_1586-61del	NP_001365402.1:n.1586-72_1586-61del
NM_001378474.1:c.1742-72_1742-61del	NP_001365403.1:n.1742-72_1742-61del
NM_001378475.1:c.1478-72_1478-61del	NP_001365404.1:n.1478-72_1478-61del