Canonical Allele Identifier: CA369543329

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140453184A>G (hg19) ; chr7:g.140753384A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753384A>G , CM000669.2:g.140753384A>G	GRCh38
NC_000007.13:g.140453184A>G , CM000669.1:g.140453184A>G	GRCh37
NC_000007.12:g.140099653A>G	NCBI36
NG_007873.3:g.176381T>C , LRG_299:g.176381T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1751T>C MANE Select	ENSP00000493543.1:p.Leu584Pro
ENST00000288602.11:c.1871T>C	ENSP00000288602.7:p.Leu624Pro
ENST00000479537.6:c.421T>C
ENST00000496384.7:c.1751T>C	ENSP00000419060.2:p.Leu584Pro
ENST00000497784.2:c.*1201T>C	ENSP00000420119.2:n.*1201T>C
ENST00000642228.1:c.*829T>C	ENSP00000493678.1:n.*829T>C
ENST00000642875.1:n.1259-3966T>C
ENST00000644120.1:n.2141T>C
ENST00000644650.1:c.847T>C
ENST00000644905.1:n.2633T>C
ENST00000644969.2:c.1871T>C MANE Plus Clinical	ENSP00000496776.1:p.Leu624Pro
ENST00000646730.1:c.*327T>C	ENSP00000494784.1:n.*327T>C
ENST00000646891.1:c.1751T>C	ENSP00000493543.1:p.Leu584Pro
ENST00000647434.1:c.738-3966T>C	ENSP00000495132.1:n.738-3966T>C
ENST00000288602.10:c.1751T>C	ENSP00000288602.6:p.Leu584Pro
ENST00000479537.5:c.35T>C	ENSP00000418033.1:p.Leu12Pro
ENST00000496384.6:c.574T>C
ENST00000497784.1:c.1786T>C	ENSP00000420119.1:n.1786T>C
NM_004333.4:c.1751T>C , LRG_299t1:c.1751T>C	NP_004324.2:p.Leu584Pro
XM_005250045.1:c.1751T>C	XP_005250102.1:p.Leu584Pro
XM_005250046.1:c.1751T>C	XP_005250103.1:p.Leu584Pro
XM_011516529.1:c.1751T>C	XP_011514831.1:p.Leu584Pro
XM_011516530.1:c.1695-3966T>C	XP_011514832.1:n.1695-3966T>C
XR_242190.1:n.1759T>C
XR_927520.1:n.1759T>C
XR_927521.1:n.1759T>C
XR_927522.1:n.1703-3966T>C
XR_927523.1:n.1703-3966T>C
NM_001354609.1:c.1751T>C	NP_001341538.1:p.Leu584Pro
NM_004333.5:c.1751T>C	NP_004324.2:p.Leu584Pro
NR_148928.1:n.2849T>C
XM_017012558.1:c.1871T>C	XP_016868047.1:p.Leu624Pro
XM_017012559.1:c.1871T>C	XP_016868048.1:p.Leu624Pro
XR_001744857.1:n.1879T>C
XR_001744858.1:n.1823-3966T>C
NM_001354609.2:c.1751T>C	NP_001341538.1:p.Leu584Pro
NM_001374244.1:c.1871T>C	NP_001361173.1:p.Leu624Pro
NM_001374258.1:c.1871T>C MANE Plus Clinical	NP_001361187.1:p.Leu624Pro
NM_004333.6:c.1751T>C MANE Select	NP_004324.2:p.Leu584Pro
NM_001378467.1:c.1760T>C	NP_001365396.1:p.Leu587Pro
NM_001378468.1:c.1751T>C	NP_001365397.1:p.Leu584Pro
NM_001378469.1:c.1685T>C	NP_001365398.1:p.Leu562Pro
NM_001378470.1:c.1649T>C	NP_001365399.1:p.Leu550Pro
NM_001378471.1:c.1640T>C	NP_001365400.1:p.Leu547Pro
NM_001378472.1:c.1595T>C	NP_001365401.1:p.Leu532Pro
NM_001378473.1:c.1595T>C	NP_001365402.1:p.Leu532Pro
NM_001378474.1:c.1751T>C	NP_001365403.1:p.Leu584Pro
NM_001378475.1:c.1487T>C	NP_001365404.1:p.Leu496Pro