Canonical Allele Identifier: CA369590862

Gene: BRAF

Linked Data

• ClinVar Variation Id: 2736869
• ClinVar RCV Id: RCV003540163
• MyVariant Identifiers: chr7:g.140501341G>C (hg19) ; chr7:g.140801541G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140801541G>C , CM000669.2:g.140801541G>C	GRCh38
NC_000007.13:g.140501341G>C , CM000669.1:g.140501341G>C	GRCh37
NC_000007.12:g.140147810G>C	NCBI36
NG_007873.3:g.128224C>G , LRG_299:g.128224C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.731C>G MANE Select	ENSP00000493543.1:p.Thr244Ser
ENST00000288602.11:c.731C>G	ENSP00000288602.7:p.Thr244Ser
ENST00000496384.7:c.731C>G	ENSP00000419060.2:p.Thr244Ser
ENST00000497784.2:c.*181C>G	ENSP00000420119.2:n.*181C>G
ENST00000642228.1:c.731C>G	ENSP00000493678.1:p.Thr244Ser
ENST00000642272.1:n.763C>G
ENST00000642875.1:n.225C>G
ENST00000643356.1:n.332C>G
ENST00000644120.1:n.1173C>G
ENST00000644905.1:n.820C>G
ENST00000644969.2:c.731C>G MANE Plus Clinical	ENSP00000496776.1:p.Thr244Ser
ENST00000646730.1:c.731C>G	ENSP00000494784.1:p.Thr244Ser
ENST00000646891.1:c.731C>G	ENSP00000493543.1:p.Thr244Ser
ENST00000288602.10:c.731C>G	ENSP00000288602.6:p.Thr244Ser
ENST00000497784.1:c.766C>G	ENSP00000420119.1:n.766C>G
NM_004333.4:c.731C>G , LRG_299t1:c.731C>G	NP_004324.2:p.Thr244Ser
XM_005250045.1:c.731C>G	XP_005250102.1:p.Thr244Ser
XM_005250046.1:c.731C>G	XP_005250103.1:p.Thr244Ser
XM_011516529.1:c.731C>G	XP_011514831.1:p.Thr244Ser
XM_011516530.1:c.731C>G	XP_011514832.1:p.Thr244Ser
XR_242190.1:n.739C>G
XR_927520.1:n.739C>G
XR_927521.1:n.739C>G
XR_927522.1:n.739C>G
XR_927523.1:n.739C>G
NM_001354609.1:c.731C>G	NP_001341538.1:p.Thr244Ser
NM_004333.5:c.731C>G	NP_004324.2:p.Thr244Ser
NR_148928.1:n.1036C>G
XM_017012558.1:c.731C>G	XP_016868047.1:p.Thr244Ser
XM_017012559.1:c.731C>G	XP_016868048.1:p.Thr244Ser
XR_001744857.1:n.739C>G
XR_001744858.1:n.739C>G
NM_001354609.2:c.731C>G	NP_001341538.1:p.Thr244Ser
NM_001374244.1:c.731C>G	NP_001361173.1:p.Thr244Ser
NM_001374258.1:c.731C>G MANE Plus Clinical	NP_001361187.1:p.Thr244Ser
NM_004333.6:c.731C>G MANE Select	NP_004324.2:p.Thr244Ser
NM_001378467.1:c.740C>G	NP_001365396.1:p.Thr247Ser
NM_001378468.1:c.731C>G	NP_001365397.1:p.Thr244Ser
NM_001378469.1:c.731C>G	NP_001365398.1:p.Thr244Ser
NM_001378470.1:c.629C>G	NP_001365399.1:p.Thr210Ser
NM_001378471.1:c.731C>G	NP_001365400.1:p.Thr244Ser
NM_001378472.1:c.575C>G	NP_001365401.1:p.Thr192Ser
NM_001378473.1:c.575C>G	NP_001365402.1:p.Thr192Ser
NM_001378474.1:c.731C>G	NP_001365403.1:p.Thr244Ser
NM_001378475.1:c.467C>G	NP_001365404.1:p.Thr156Ser