Canonical Allele Identifier: CA439292089

Gene: KIT

Linked Data

• COSMIC: COSM21305
• MyVariant Identifiers: chr4:g.55602756T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54736590T>G , CM000666.2:g.54736590T>G	GRCh38
NC_000004.11:g.55602756T>G , CM000666.1:g.55602756T>G	GRCh37
NC_000004.10:g.55297513T>G	NCBI36
NG_007456.1:g.83596T>G , LRG_307:g.83596T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.2565T>G	ENSP00000390987.3:p.Leu855=
ENST00000684818.1:n.1269T>G
ENST00000685269.1:n.2655T>G
ENST00000686011.1:c.2562T>G	ENSP00000509704.1:p.Leu854=
ENST00000687109.1:c.2580T>G	ENSP00000509371.1:p.Leu860=
ENST00000687208.1:n.2989T>G
ENST00000687246.1:c.2442T>G	ENSP00000509114.1:p.Leu814=
ENST00000687265.1:n.2735T>G
ENST00000687295.1:c.2565T>G	ENSP00000509450.1:p.Leu855=
ENST00000688060.1:n.374T>G
ENST00000689832.1:c.2577T>G	ENSP00000509084.1:p.Leu859=
ENST00000689994.1:c.2067T>G	ENSP00000509156.1:p.Leu689=
ENST00000690543.1:c.2568T>G	ENSP00000508831.1:p.Leu856=
ENST00000690917.1:n.2795T>G
ENST00000691361.1:n.1487T>G
ENST00000692301.1:n.1269T>G
ENST00000692783.1:c.2574T>G	ENSP00000508733.1:p.Leu858=
ENST00000692991.1:n.2674T>G
ENST00000288135.6:c.2577T>G MANE Select	ENSP00000288135.6:p.Leu859=
ENST00000288135.5:c.2577T>G	ENSP00000288135.5:p.Leu859=
ENST00000412167.6:c.2565T>G	ENSP00000390987.2:p.Leu855=
NM_000222.2:c.2577T>G , LRG_307t1:c.2577T>G	NP_000213.1:p.Leu859=
NM_001093772.1:c.2565T>G	NP_001087241.1:p.Leu855=
XM_005265740.1:c.2580T>G	XP_005265797.1:p.Leu860=
XM_005265741.1:c.2577T>G	XP_005265798.1:p.Leu859=
XM_005265742.1:c.2568T>G	XP_005265799.1:p.Leu856=
XM_005265742.3:c.2568T>G	XP_005265799.1:p.Leu856=
XM_017008178.1:c.2574T>G	XP_016863667.1:p.Leu858=
XM_017008179.1:c.2565T>G	XP_016863668.1:p.Leu855=
XM_017008180.1:c.2562T>G	XP_016863669.1:p.Leu854=
NM_000222.3:c.2577T>G MANE Select	NP_000213.1:p.Leu859=
NM_001093772.2:c.2565T>G	NP_001087241.1:p.Leu855=
NM_001385284.1:c.2580T>G	NP_001372213.1:p.Leu860=
NM_001385285.1:c.2574T>G	NP_001372214.1:p.Leu858=
NM_001385286.1:c.2562T>G	NP_001372215.1:p.Leu854=
NM_001385288.1:c.2568T>G	NP_001372217.1:p.Leu856=
NM_001385290.1:c.2577T>G	NP_001372219.1:p.Leu859=
NM_001385292.1:c.2565T>G	NP_001372221.1:p.Leu855=