Canonical Allele Identifier: CA1747732313

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140801007_140801008delinsTG , CM000669.2:g.140801007_140801008delinsTG	GRCh38
NC_000007.13:g.140500807_140500808delinsTG , CM000669.1:g.140500807_140500808delinsTG	GRCh37
NC_000007.12:g.140147276_140147277delinsTG	NCBI36
NG_007873.3:g.128757_128758delinsCA , LRG_299:g.128757_128758delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.860+404_860+405delinsCA MANE Select	ENSP00000493543.1:n.860+404_860+405delinsCA
ENST00000288602.11:c.860+404_860+405delinsCA	ENSP00000288602.7:n.860+404_860+405delinsCA
ENST00000496384.7:c.860+404_860+405delinsCA	ENSP00000419060.2:n.860+404_860+405delinsCA
ENST00000497784.2:c.*310+404_*310+405delinsCA	ENSP00000420119.2:n.*310+404_*310+405delinsCA
ENST00000642228.1:c.860+404_860+405delinsCA	ENSP00000493678.1:n.860+404_860+405delinsCA
ENST00000642272.1:n.892+404_892+405delinsCA
ENST00000642875.1:n.354+404_354+405delinsCA
ENST00000644120.1:n.1302+404_1302+405delinsCA
ENST00000644905.1:n.949+404_949+405delinsCA
ENST00000644969.2:c.860+404_860+405delinsCA MANE Plus Clinical	ENSP00000496776.1:n.860+404_860+405delinsCA
ENST00000646730.1:c.860+404_860+405delinsCA	ENSP00000494784.1:n.860+404_860+405delinsCA
ENST00000646891.1:c.860+404_860+405delinsCA	ENSP00000493543.1:n.860+404_860+405delinsCA
ENST00000288602.10:c.860+404_860+405delinsCA	ENSP00000288602.6:n.860+404_860+405delinsCA
ENST00000497784.1:c.895+404_895+405delinsCA	ENSP00000420119.1:n.895+404_895+405delinsCA
NM_004333.4:c.860+404_860+405delinsCA , LRG_299t1:c.860+404_860+405delinsCA	NP_004324.2:n.860+404_860+405delinsCA
XM_005250045.1:c.860+404_860+405delinsCA	XP_005250102.1:n.860+404_860+405delinsCA
XM_005250046.1:c.860+404_860+405delinsCA	XP_005250103.1:n.860+404_860+405delinsCA
XM_011516529.1:c.860+404_860+405delinsCA	XP_011514831.1:n.860+404_860+405delinsCA
XM_011516530.1:c.860+404_860+405delinsCA	XP_011514832.1:n.860+404_860+405delinsCA
XR_242190.1:n.868+404_868+405delinsCA
XR_927520.1:n.868+404_868+405delinsCA
XR_927521.1:n.868+404_868+405delinsCA
XR_927522.1:n.868+404_868+405delinsCA
XR_927523.1:n.868+404_868+405delinsCA
NM_001354609.1:c.860+404_860+405delinsCA	NP_001341538.1:n.860+404_860+405delinsCA
NM_004333.5:c.860+404_860+405delinsCA	NP_004324.2:n.860+404_860+405delinsCA
NR_148928.1:n.1165+404_1165+405delinsCA
XM_017012558.1:c.860+404_860+405delinsCA	XP_016868047.1:n.860+404_860+405delinsCA
XM_017012559.1:c.860+404_860+405delinsCA	XP_016868048.1:n.860+404_860+405delinsCA
XR_001744857.1:n.868+404_868+405delinsCA
XR_001744858.1:n.868+404_868+405delinsCA
NM_001354609.2:c.860+404_860+405delinsCA	NP_001341538.1:n.860+404_860+405delinsCA
NM_001374244.1:c.860+404_860+405delinsCA	NP_001361173.1:n.860+404_860+405delinsCA
NM_001374258.1:c.860+404_860+405delinsCA MANE Plus Clinical	NP_001361187.1:n.860+404_860+405delinsCA
NM_004333.6:c.860+404_860+405delinsCA MANE Select	NP_004324.2:n.860+404_860+405delinsCA
NM_001378467.1:c.869+404_869+405delinsCA	NP_001365396.1:n.869+404_869+405delinsCA
NM_001378468.1:c.860+404_860+405delinsCA	NP_001365397.1:n.860+404_860+405delinsCA
NM_001378469.1:c.860+404_860+405delinsCA	NP_001365398.1:n.860+404_860+405delinsCA
NM_001378470.1:c.758+404_758+405delinsCA	NP_001365399.1:n.758+404_758+405delinsCA
NM_001378471.1:c.860+404_860+405delinsCA	NP_001365400.1:n.860+404_860+405delinsCA
NM_001378472.1:c.704+404_704+405delinsCA	NP_001365401.1:n.704+404_704+405delinsCA
NM_001378473.1:c.704+404_704+405delinsCA	NP_001365402.1:n.704+404_704+405delinsCA
NM_001378474.1:c.860+404_860+405delinsCA	NP_001365403.1:n.860+404_860+405delinsCA
NM_001378475.1:c.596+404_596+405delinsCA	NP_001365404.1:n.596+404_596+405delinsCA