Canonical Allele Identifier: CA2685244391

Gene: BRAF

Linked Data

• gnomAD v4: 7-140801540-G-GGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140801541_140801542insCTG , CM000669.2:g.140801541_140801542insCTG	GRCh38
NC_000007.13:g.140501341_140501342insCTG , CM000669.1:g.140501341_140501342insCTG	GRCh37
NC_000007.12:g.140147810_140147811insCTG	NCBI36
NG_007873.3:g.128224_128225insAGC , LRG_299:g.128224_128225insAGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.731_732insAGC MANE Select	ENSP00000493543.1:p.Thr244_Leu245insAla
ENST00000288602.11:c.731_732insAGC	ENSP00000288602.7:p.Thr244_Leu245insAla
ENST00000496384.7:c.731_732insAGC	ENSP00000419060.2:p.Thr244_Leu245insAla
ENST00000497784.2:c.*181_*182insAGC	ENSP00000420119.2:n.*181_*182insAGC
ENST00000642228.1:c.731_732insAGC	ENSP00000493678.1:p.Thr244_Leu245insAla
ENST00000642272.1:n.763_764insAGC
ENST00000642875.1:n.225_226insAGC
ENST00000643356.1:n.332_333insAGC
ENST00000644120.1:n.1173_1174insAGC
ENST00000644905.1:n.820_821insAGC
ENST00000644969.2:c.731_732insAGC MANE Plus Clinical	ENSP00000496776.1:p.Thr244_Leu245insAla
ENST00000646730.1:c.731_732insAGC	ENSP00000494784.1:p.Thr244_Leu245insAla
ENST00000646891.1:c.731_732insAGC	ENSP00000493543.1:p.Thr244_Leu245insAla
ENST00000288602.10:c.731_732insAGC	ENSP00000288602.6:p.Thr244_Leu245insAla
ENST00000497784.1:c.766_767insAGC	ENSP00000420119.1:n.766_767insAGC
NM_004333.4:c.731_732insAGC , LRG_299t1:c.731_732insAGC	NP_004324.2:p.Thr244_Leu245insAla
XM_005250045.1:c.731_732insAGC	XP_005250102.1:p.Thr244_Leu245insAla
XM_005250046.1:c.731_732insAGC	XP_005250103.1:p.Thr244_Leu245insAla
XM_011516529.1:c.731_732insAGC	XP_011514831.1:p.Thr244_Leu245insAla
XM_011516530.1:c.731_732insAGC	XP_011514832.1:p.Thr244_Leu245insAla
XR_242190.1:n.739_740insAGC
XR_927520.1:n.739_740insAGC
XR_927521.1:n.739_740insAGC
XR_927522.1:n.739_740insAGC
XR_927523.1:n.739_740insAGC
NM_001354609.1:c.731_732insAGC	NP_001341538.1:p.Thr244_Leu245insAla
NM_004333.5:c.731_732insAGC	NP_004324.2:p.Thr244_Leu245insAla
NR_148928.1:n.1036_1037insAGC
XM_017012558.1:c.731_732insAGC	XP_016868047.1:p.Thr244_Leu245insAla
XM_017012559.1:c.731_732insAGC	XP_016868048.1:p.Thr244_Leu245insAla
XR_001744857.1:n.739_740insAGC
XR_001744858.1:n.739_740insAGC
NM_001354609.2:c.731_732insAGC	NP_001341538.1:p.Thr244_Leu245insAla
NM_001374244.1:c.731_732insAGC	NP_001361173.1:p.Thr244_Leu245insAla
NM_001374258.1:c.731_732insAGC MANE Plus Clinical	NP_001361187.1:p.Thr244_Leu245insAla
NM_004333.6:c.731_732insAGC MANE Select	NP_004324.2:p.Thr244_Leu245insAla
NM_001378467.1:c.740_741insAGC	NP_001365396.1:p.Thr247_Leu248insAla
NM_001378468.1:c.731_732insAGC	NP_001365397.1:p.Thr244_Leu245insAla
NM_001378469.1:c.731_732insAGC	NP_001365398.1:p.Thr244_Leu245insAla
NM_001378470.1:c.629_630insAGC	NP_001365399.1:p.Thr210_Leu211insAla
NM_001378471.1:c.731_732insAGC	NP_001365400.1:p.Thr244_Leu245insAla
NM_001378472.1:c.575_576insAGC	NP_001365401.1:p.Thr192_Leu193insAla
NM_001378473.1:c.575_576insAGC	NP_001365402.1:p.Thr192_Leu193insAla
NM_001378474.1:c.731_732insAGC	NP_001365403.1:p.Thr244_Leu245insAla
NM_001378475.1:c.467_468insAGC	NP_001365404.1:p.Thr156_Leu157insAla