Canonical Allele Identifier: CA2685224002

Gene: BRAF

Linked Data

• gnomAD v4: 7-140753421-GTAGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753423_140753426del , CM000669.2:g.140753423_140753426del	GRCh38
NC_000007.13:g.140453223_140453226del , CM000669.1:g.140453223_140453226del	GRCh37
NC_000007.12:g.140099692_140099695del	NCBI36
NG_007873.3:g.176340_176343del , LRG_299:g.176340_176343del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1742-32_1742-29del MANE Select	ENSP00000493543.1:n.1742-32_1742-29del
ENST00000288602.11:c.1862-32_1862-29del	ENSP00000288602.7:n.1862-32_1862-29del
ENST00000479537.6:c.412-32_412-29del
ENST00000496384.7:c.1742-32_1742-29del	ENSP00000419060.2:n.1742-32_1742-29del
ENST00000497784.2:c.*1192-32_*1192-29del	ENSP00000420119.2:n.*1192-32_*1192-29del
ENST00000642228.1:c.*820-32_*820-29del	ENSP00000493678.1:n.*820-32_*820-29del
ENST00000642875.1:n.1259-4007_1259-4004del
ENST00000644120.1:n.2132-32_2132-29del
ENST00000644650.1:c.838-32_838-29del
ENST00000644905.1:n.2592_2595del
ENST00000644969.2:c.1862-32_1862-29del MANE Plus Clinical	ENSP00000496776.1:n.1862-32_1862-29del
ENST00000646730.1:c.*318-32_*318-29del	ENSP00000494784.1:n.*318-32_*318-29del
ENST00000646891.1:c.1742-32_1742-29del	ENSP00000493543.1:n.1742-32_1742-29del
ENST00000647434.1:c.738-4007_738-4004del	ENSP00000495132.1:n.738-4007_738-4004del
ENST00000288602.10:c.1742-32_1742-29del	ENSP00000288602.6:n.1742-32_1742-29del
ENST00000479537.5:c.26-32_26-29del	ENSP00000418033.1:n.26-32_26-29del
ENST00000496384.6:c.565-32_565-29del
ENST00000497784.1:c.1777-32_1777-29del	ENSP00000420119.1:n.1777-32_1777-29del
NM_004333.4:c.1742-32_1742-29del , LRG_299t1:c.1742-32_1742-29del	NP_004324.2:n.1742-32_1742-29del
XM_005250045.1:c.1742-32_1742-29del	XP_005250102.1:n.1742-32_1742-29del
XM_005250046.1:c.1742-32_1742-29del	XP_005250103.1:n.1742-32_1742-29del
XM_011516529.1:c.1742-32_1742-29del	XP_011514831.1:n.1742-32_1742-29del
XM_011516530.1:c.1695-4007_1695-4004del	XP_011514832.1:n.1695-4007_1695-4004del
XR_242190.1:n.1750-32_1750-29del
XR_927520.1:n.1750-32_1750-29del
XR_927521.1:n.1750-32_1750-29del
XR_927522.1:n.1703-4007_1703-4004del
XR_927523.1:n.1703-4007_1703-4004del
NM_001354609.1:c.1742-32_1742-29del	NP_001341538.1:n.1742-32_1742-29del
NM_004333.5:c.1742-32_1742-29del	NP_004324.2:n.1742-32_1742-29del
NR_148928.1:n.2808_2811del
XM_017012558.1:c.1862-32_1862-29del	XP_016868047.1:n.1862-32_1862-29del
XM_017012559.1:c.1862-32_1862-29del	XP_016868048.1:n.1862-32_1862-29del
XR_001744857.1:n.1870-32_1870-29del
XR_001744858.1:n.1823-4007_1823-4004del
NM_001354609.2:c.1742-32_1742-29del	NP_001341538.1:n.1742-32_1742-29del
NM_001374244.1:c.1862-32_1862-29del	NP_001361173.1:n.1862-32_1862-29del
NM_001374258.1:c.1862-32_1862-29del MANE Plus Clinical	NP_001361187.1:n.1862-32_1862-29del
NM_004333.6:c.1742-32_1742-29del MANE Select	NP_004324.2:n.1742-32_1742-29del
NM_001378467.1:c.1751-32_1751-29del	NP_001365396.1:n.1751-32_1751-29del
NM_001378468.1:c.1742-32_1742-29del	NP_001365397.1:n.1742-32_1742-29del
NM_001378469.1:c.1676-32_1676-29del	NP_001365398.1:n.1676-32_1676-29del
NM_001378470.1:c.1640-32_1640-29del	NP_001365399.1:n.1640-32_1640-29del
NM_001378471.1:c.1631-32_1631-29del	NP_001365400.1:n.1631-32_1631-29del
NM_001378472.1:c.1586-32_1586-29del	NP_001365401.1:n.1586-32_1586-29del
NM_001378473.1:c.1586-32_1586-29del	NP_001365402.1:n.1586-32_1586-29del
NM_001378474.1:c.1742-32_1742-29del	NP_001365403.1:n.1742-32_1742-29del
NM_001378475.1:c.1478-32_1478-29del	NP_001365404.1:n.1478-32_1478-29del