Canonical Allele Identifier: CA356913331

Gene: KIT

Linked Data

• MyVariant Identifiers: chr4:g.55602751T>G (hg19) ; chr4:g.54736585T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54736585T>G , CM000666.2:g.54736585T>G	GRCh38
NC_000004.11:g.55602751T>G , CM000666.1:g.55602751T>G	GRCh37
NC_000004.10:g.55297508T>G	NCBI36
NG_007456.1:g.83591T>G , LRG_307:g.83591T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.2560T>G	ENSP00000390987.3:p.Phe854Val
ENST00000684818.1:n.1264T>G
ENST00000685269.1:n.2650T>G
ENST00000686011.1:c.2557T>G	ENSP00000509704.1:p.Phe853Val
ENST00000687109.1:c.2575T>G	ENSP00000509371.1:p.Phe859Val
ENST00000687208.1:n.2984T>G
ENST00000687246.1:c.2437T>G	ENSP00000509114.1:p.Phe813Val
ENST00000687265.1:n.2730T>G
ENST00000687295.1:c.2560T>G	ENSP00000509450.1:p.Phe854Val
ENST00000688060.1:n.369T>G
ENST00000689832.1:c.2572T>G	ENSP00000509084.1:p.Phe858Val
ENST00000689994.1:c.2062T>G	ENSP00000509156.1:p.Phe688Val
ENST00000690543.1:c.2563T>G	ENSP00000508831.1:p.Phe855Val
ENST00000690917.1:n.2790T>G
ENST00000691361.1:n.1482T>G
ENST00000692301.1:n.1264T>G
ENST00000692783.1:c.2569T>G	ENSP00000508733.1:p.Phe857Val
ENST00000692991.1:n.2669T>G
ENST00000288135.6:c.2572T>G MANE Select	ENSP00000288135.6:p.Phe858Val
ENST00000288135.5:c.2572T>G	ENSP00000288135.5:p.Phe858Val
ENST00000412167.6:c.2560T>G	ENSP00000390987.2:p.Phe854Val
NM_000222.2:c.2572T>G , LRG_307t1:c.2572T>G	NP_000213.1:p.Phe858Val
NM_001093772.1:c.2560T>G	NP_001087241.1:p.Phe854Val
XM_005265740.1:c.2575T>G	XP_005265797.1:p.Phe859Val
XM_005265741.1:c.2572T>G	XP_005265798.1:p.Phe858Val
XM_005265742.1:c.2563T>G	XP_005265799.1:p.Phe855Val
XM_005265742.3:c.2563T>G	XP_005265799.1:p.Phe855Val
XM_017008178.1:c.2569T>G	XP_016863667.1:p.Phe857Val
XM_017008179.1:c.2560T>G	XP_016863668.1:p.Phe854Val
XM_017008180.1:c.2557T>G	XP_016863669.1:p.Phe853Val
NM_000222.3:c.2572T>G MANE Select	NP_000213.1:p.Phe858Val
NM_001093772.2:c.2560T>G	NP_001087241.1:p.Phe854Val
NM_001385284.1:c.2575T>G	NP_001372213.1:p.Phe859Val
NM_001385285.1:c.2569T>G	NP_001372214.1:p.Phe857Val
NM_001385286.1:c.2557T>G	NP_001372215.1:p.Phe853Val
NM_001385288.1:c.2563T>G	NP_001372217.1:p.Phe855Val
NM_001385290.1:c.2572T>G	NP_001372219.1:p.Phe858Val
NM_001385292.1:c.2560T>G	NP_001372221.1:p.Phe854Val