Canonical Allele Identifier: CA369590543

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140500274A>G (hg19) ; chr7:g.140800474A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140800474A>G , CM000669.2:g.140800474A>G	GRCh38
NC_000007.13:g.140500274A>G , CM000669.1:g.140500274A>G	GRCh37
NC_000007.12:g.140146743A>G	NCBI36
NG_007873.3:g.129291T>C , LRG_299:g.129291T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.868T>C MANE Select	ENSP00000493543.1:p.Phe290Leu
ENST00000288602.11:c.868T>C	ENSP00000288602.7:p.Phe290Leu
ENST00000496384.7:c.868T>C	ENSP00000419060.2:p.Phe290Leu
ENST00000497784.2:c.*318T>C	ENSP00000420119.2:n.*318T>C
ENST00000642228.1:c.861-12T>C	ENSP00000493678.1:n.861-12T>C
ENST00000642272.1:n.900T>C
ENST00000642875.1:n.362T>C
ENST00000644120.1:n.1310T>C
ENST00000644905.1:n.957T>C
ENST00000644969.2:c.868T>C MANE Plus Clinical	ENSP00000496776.1:p.Phe290Leu
ENST00000646730.1:c.868T>C	ENSP00000494784.1:p.Phe290Leu
ENST00000646891.1:c.868T>C	ENSP00000493543.1:p.Phe290Leu
ENST00000288602.10:c.868T>C	ENSP00000288602.6:p.Phe290Leu
ENST00000497784.1:c.903T>C	ENSP00000420119.1:n.903T>C
NM_004333.4:c.868T>C , LRG_299t1:c.868T>C	NP_004324.2:p.Phe290Leu
XM_005250045.1:c.868T>C	XP_005250102.1:p.Phe290Leu
XM_005250046.1:c.868T>C	XP_005250103.1:p.Phe290Leu
XM_011516529.1:c.868T>C	XP_011514831.1:p.Phe290Leu
XM_011516530.1:c.868T>C	XP_011514832.1:p.Phe290Leu
XR_242190.1:n.876T>C
XR_927520.1:n.876T>C
XR_927521.1:n.876T>C
XR_927522.1:n.876T>C
XR_927523.1:n.876T>C
NM_001354609.1:c.868T>C	NP_001341538.1:p.Phe290Leu
NM_004333.5:c.868T>C	NP_004324.2:p.Phe290Leu
NR_148928.1:n.1173T>C
XM_017012558.1:c.868T>C	XP_016868047.1:p.Phe290Leu
XM_017012559.1:c.868T>C	XP_016868048.1:p.Phe290Leu
XR_001744857.1:n.876T>C
XR_001744858.1:n.876T>C
NM_001354609.2:c.868T>C	NP_001341538.1:p.Phe290Leu
NM_001374244.1:c.868T>C	NP_001361173.1:p.Phe290Leu
NM_001374258.1:c.868T>C MANE Plus Clinical	NP_001361187.1:p.Phe290Leu
NM_004333.6:c.868T>C MANE Select	NP_004324.2:p.Phe290Leu
NM_001378467.1:c.877T>C	NP_001365396.1:p.Phe293Leu
NM_001378468.1:c.868T>C	NP_001365397.1:p.Phe290Leu
NM_001378469.1:c.868T>C	NP_001365398.1:p.Phe290Leu
NM_001378470.1:c.766T>C	NP_001365399.1:p.Phe256Leu
NM_001378471.1:c.868T>C	NP_001365400.1:p.Phe290Leu
NM_001378472.1:c.712T>C	NP_001365401.1:p.Phe238Leu
NM_001378473.1:c.712T>C	NP_001365402.1:p.Phe238Leu
NM_001378474.1:c.868T>C	NP_001365403.1:p.Phe290Leu
NM_001378475.1:c.604T>C	NP_001365404.1:p.Phe202Leu