Canonical Allele Identifier: CA439291272
Gene: KIT HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.55593665T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54727499T>G , CM000666.2:g.54727499T>G GRCh38
NC_000004.11:g.55593665T>G , CM000666.1:g.55593665T>G GRCh37
NC_000004.10:g.55288422T>G NCBI36
NG_007456.1:g.74505T>G , LRG_307:g.74505T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000412167.7:c.1722T>G ENSP00000390987.3:p.Pro574=
ENST00000685269.1:n.1809T>G
ENST00000686011.1:c.1719T>G ENSP00000509704.1:p.Pro573=
ENST00000687109.1:c.1734T>G ENSP00000509371.1:p.Pro578=
ENST00000687208.1:n.2146T>G
ENST00000687246.1:c.1719T>G ENSP00000509114.1:p.Pro573=
ENST00000687265.1:n.1889T>G
ENST00000687295.1:c.1719T>G ENSP00000509450.1:p.Pro573=
ENST00000689832.1:c.1734T>G ENSP00000509084.1:p.Pro578=
ENST00000689994.1:c.1221T>G ENSP00000509156.1:p.Pro407=
ENST00000690543.1:c.1722T>G ENSP00000508831.1:p.Pro574=
ENST00000690917.1:n.1949T>G
ENST00000691361.1:n.641T>G
ENST00000692783.1:c.1731T>G ENSP00000508733.1:p.Pro577=
ENST00000692991.1:n.1828T>G
ENST00000288135.6:c.1731T>G MANE Select ENSP00000288135.6:p.Pro577=
ENST00000288135.5:c.1731T>G ENSP00000288135.5:p.Pro577=
ENST00000412167.6:c.1719T>G ENSP00000390987.2:p.Pro573=
NM_000222.2:c.1731T>G , LRG_307t1:c.1731T>G NP_000213.1:p.Pro577=
NM_001093772.1:c.1719T>G NP_001087241.1:p.Pro573=
XM_005265740.1:c.1734T>G XP_005265797.1:p.Pro578=
XM_005265741.1:c.1734T>G XP_005265798.1:p.Pro578=
XM_005265742.1:c.1722T>G XP_005265799.1:p.Pro574=
XM_005265742.3:c.1722T>G XP_005265799.1:p.Pro574=
XM_017008178.1:c.1731T>G XP_016863667.1:p.Pro577=
XM_017008179.1:c.1722T>G XP_016863668.1:p.Pro574=
XM_017008180.1:c.1719T>G XP_016863669.1:p.Pro573=
NM_000222.3:c.1731T>G MANE Select NP_000213.1:p.Pro577=
NM_001093772.2:c.1719T>G NP_001087241.1:p.Pro573=
NM_001385284.1:c.1734T>G NP_001372213.1:p.Pro578=
NM_001385285.1:c.1731T>G NP_001372214.1:p.Pro577=
NM_001385286.1:c.1719T>G NP_001372215.1:p.Pro573=
NM_001385288.1:c.1722T>G NP_001372217.1:p.Pro574=
NM_001385290.1:c.1734T>G NP_001372219.1:p.Pro578=
NM_001385292.1:c.1722T>G NP_001372221.1:p.Pro574=