Canonical Allele Identifier: CA369542819

Gene: BRAF

Linked Data

• dbSNP Id: rs781529187
• COSMIC: COSM27931
• MyVariant Identifiers: chr7:g.140453101G>A (hg19) ; chr7:g.140753301G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753301G>A , CM000669.2:g.140753301G>A	GRCh38
NC_000007.13:g.140453101G>A , CM000669.1:g.140453101G>A	GRCh37
NC_000007.12:g.140099570G>A	NCBI36
NG_007873.3:g.176464C>T , LRG_299:g.176464C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1834C>T MANE Select	ENSP00000493543.1:p.Gln612Ter
ENST00000288602.11:c.1954C>T	ENSP00000288602.7:p.Gln652Ter
ENST00000479537.6:c.504C>T
ENST00000496384.7:c.1834C>T	ENSP00000419060.2:p.Gln612Ter
ENST00000497784.2:c.*1284C>T	ENSP00000420119.2:n.*1284C>T
ENST00000642228.1:c.*912C>T	ENSP00000493678.1:n.*912C>T
ENST00000642875.1:n.1259-3883C>T
ENST00000644120.1:n.2224C>T
ENST00000644650.1:c.930C>T
ENST00000644905.1:n.2716C>T
ENST00000644969.2:c.1954C>T MANE Plus Clinical	ENSP00000496776.1:p.Gln652Ter
ENST00000646730.1:c.*410C>T	ENSP00000494784.1:n.*410C>T
ENST00000646891.1:c.1834C>T	ENSP00000493543.1:p.Gln612Ter
ENST00000647434.1:c.738-3883C>T	ENSP00000495132.1:n.738-3883C>T
ENST00000288602.10:c.1834C>T	ENSP00000288602.6:p.Gln612Ter
ENST00000479537.5:c.118C>T	ENSP00000418033.1:p.Gln40Ter
ENST00000496384.6:c.657C>T
ENST00000497784.1:c.1869C>T	ENSP00000420119.1:n.1869C>T
NM_004333.4:c.1834C>T , LRG_299t1:c.1834C>T	NP_004324.2:p.Gln612Ter
XM_005250045.1:c.1834C>T	XP_005250102.1:p.Gln612Ter
XM_005250046.1:c.1834C>T	XP_005250103.1:p.Gln612Ter
XM_011516529.1:c.1834C>T	XP_011514831.1:p.Gln612Ter
XM_011516530.1:c.1695-3883C>T	XP_011514832.1:n.1695-3883C>T
XR_242190.1:n.1842C>T
XR_927520.1:n.1842C>T
XR_927521.1:n.1842C>T
XR_927522.1:n.1703-3883C>T
XR_927523.1:n.1703-3883C>T
NM_001354609.1:c.1834C>T	NP_001341538.1:p.Gln612Ter
NM_004333.5:c.1834C>T	NP_004324.2:p.Gln612Ter
NR_148928.1:n.2932C>T
XM_017012558.1:c.1954C>T	XP_016868047.1:p.Gln652Ter
XM_017012559.1:c.1954C>T	XP_016868048.1:p.Gln652Ter
XR_001744857.1:n.1962C>T
XR_001744858.1:n.1823-3883C>T
NM_001354609.2:c.1834C>T	NP_001341538.1:p.Gln612Ter
NM_001374244.1:c.1954C>T	NP_001361173.1:p.Gln652Ter
NM_001374258.1:c.1954C>T MANE Plus Clinical	NP_001361187.1:p.Gln652Ter
NM_004333.6:c.1834C>T MANE Select	NP_004324.2:p.Gln612Ter
NM_001378467.1:c.1843C>T	NP_001365396.1:p.Gln615Ter
NM_001378468.1:c.1834C>T	NP_001365397.1:p.Gln612Ter
NM_001378469.1:c.1768C>T	NP_001365398.1:p.Gln590Ter
NM_001378470.1:c.1732C>T	NP_001365399.1:p.Gln578Ter
NM_001378471.1:c.1723C>T	NP_001365400.1:p.Gln575Ter
NM_001378472.1:c.1678C>T	NP_001365401.1:p.Gln560Ter
NM_001378473.1:c.1678C>T	NP_001365402.1:p.Gln560Ter
NM_001378474.1:c.1834C>T	NP_001365403.1:p.Gln612Ter
NM_001378475.1:c.1570C>T	NP_001365404.1:p.Gln524Ter