Canonical Allele Identifier: CA1747709993

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753321_140753322delinsCT , CM000669.2:g.140753321_140753322delinsCT	GRCh38
NC_000007.13:g.140453121_140453122delinsCT , CM000669.1:g.140453121_140453122delinsCT	GRCh37
NC_000007.12:g.140099590_140099591delinsCT	NCBI36
NG_007873.3:g.176443_176444delinsAG , LRG_299:g.176443_176444delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1813_1814delinsAG MANE Select	ENSP00000493543.1:p.Ser605=
ENST00000288602.11:c.1933_1934delinsAG	ENSP00000288602.7:p.Ser645=
ENST00000479537.6:c.483_484delinsAG
ENST00000496384.7:c.1813_1814delinsAG	ENSP00000419060.2:p.Ser605=
ENST00000497784.2:c.*1263_*1264delinsAG	ENSP00000420119.2:n.*1263_*1264delinsAG
ENST00000642228.1:c.*891_*892delinsAG	ENSP00000493678.1:n.*891_*892delinsAG
ENST00000642875.1:n.1259-3904_1259-3903delinsAG
ENST00000644120.1:n.2203_2204delinsAG
ENST00000644650.1:c.909_910delinsAG
ENST00000644905.1:n.2695_2696delinsAG
ENST00000644969.2:c.1933_1934delinsAG MANE Plus Clinical	ENSP00000496776.1:p.Ser645=
ENST00000646730.1:c.*389_*390delinsAG	ENSP00000494784.1:n.*389_*390delinsAG
ENST00000646891.1:c.1813_1814delinsAG	ENSP00000493543.1:p.Ser605=
ENST00000647434.1:c.738-3904_738-3903delinsAG	ENSP00000495132.1:n.738-3904_738-3903delinsAG
ENST00000288602.10:c.1813_1814delinsAG	ENSP00000288602.6:p.Ser605=
ENST00000479537.5:c.97_98delinsAG	ENSP00000418033.1:p.Ser33=
ENST00000496384.6:c.636_637delinsAG
ENST00000497784.1:c.1848_1849delinsAG	ENSP00000420119.1:n.1848_1849delinsAG
NM_004333.4:c.1813_1814delinsAG , LRG_299t1:c.1813_1814delinsAG	NP_004324.2:p.Ser605=
XM_005250045.1:c.1813_1814delinsAG	XP_005250102.1:p.Ser605=
XM_005250046.1:c.1813_1814delinsAG	XP_005250103.1:p.Ser605=
XM_011516529.1:c.1813_1814delinsAG	XP_011514831.1:p.Ser605=
XM_011516530.1:c.1695-3904_1695-3903delinsAG	XP_011514832.1:n.1695-3904_1695-3903delinsAG
XR_242190.1:n.1821_1822delinsAG
XR_927520.1:n.1821_1822delinsAG
XR_927521.1:n.1821_1822delinsAG
XR_927522.1:n.1703-3904_1703-3903delinsAG
XR_927523.1:n.1703-3904_1703-3903delinsAG
NM_001354609.1:c.1813_1814delinsAG	NP_001341538.1:p.Ser605=
NM_004333.5:c.1813_1814delinsAG	NP_004324.2:p.Ser605=
NR_148928.1:n.2911_2912delinsAG
XM_017012558.1:c.1933_1934delinsAG	XP_016868047.1:p.Ser645=
XM_017012559.1:c.1933_1934delinsAG	XP_016868048.1:p.Ser645=
XR_001744857.1:n.1941_1942delinsAG
XR_001744858.1:n.1823-3904_1823-3903delinsAG
NM_001354609.2:c.1813_1814delinsAG	NP_001341538.1:p.Ser605=
NM_001374244.1:c.1933_1934delinsAG	NP_001361173.1:p.Ser645=
NM_001374258.1:c.1933_1934delinsAG MANE Plus Clinical	NP_001361187.1:p.Ser645=
NM_004333.6:c.1813_1814delinsAG MANE Select	NP_004324.2:p.Ser605=
NM_001378467.1:c.1822_1823delinsAG	NP_001365396.1:p.Ser608=
NM_001378468.1:c.1813_1814delinsAG	NP_001365397.1:p.Ser605=
NM_001378469.1:c.1747_1748delinsAG	NP_001365398.1:p.Ser583=
NM_001378470.1:c.1711_1712delinsAG	NP_001365399.1:p.Ser571=
NM_001378471.1:c.1702_1703delinsAG	NP_001365400.1:p.Ser568=
NM_001378472.1:c.1657_1658delinsAG	NP_001365401.1:p.Ser553=
NM_001378473.1:c.1657_1658delinsAG	NP_001365402.1:p.Ser553=
NM_001378474.1:c.1813_1814delinsAG	NP_001365403.1:p.Ser605=
NM_001378475.1:c.1549_1550delinsAG	NP_001365404.1:p.Ser517=