Canonical Allele Identifier: CA551651641

Gene: KIT

Linked Data

• dbSNP Id: rs1396758170
• gnomAD v2: 4-55593758-CAG-C
• gnomAD v4: 4-54727592-CAG-C
• MyVariant Identifiers: chr4:g.55593759_55593760del (hg19) ; chr4:g.54727593_54727594del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727593_54727594del , CM000666.2:g.54727593_54727594del	GRCh38
NC_000004.11:g.55593759_55593760del , CM000666.1:g.55593759_55593760del	GRCh37
NC_000004.10:g.55288516_55288517del	NCBI36
NG_007456.1:g.74599_74600del , LRG_307:g.74599_74600del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1765+51_1765+52del	ENSP00000390987.3:n.1765+51_1765+52del
ENST00000685269.1:n.1852+51_1852+52del
ENST00000686011.1:c.1762+51_1762+52del	ENSP00000509704.1:n.1762+51_1762+52del
ENST00000687109.1:c.1777+51_1777+52del	ENSP00000509371.1:n.1777+51_1777+52del
ENST00000687208.1:n.2189+51_2189+52del
ENST00000687246.1:c.1762+51_1762+52del	ENSP00000509114.1:n.1762+51_1762+52del
ENST00000687265.1:n.1932+51_1932+52del
ENST00000687295.1:c.1762+51_1762+52del	ENSP00000509450.1:n.1762+51_1762+52del
ENST00000689832.1:c.1777+51_1777+52del	ENSP00000509084.1:n.1777+51_1777+52del
ENST00000689994.1:c.1264+51_1264+52del	ENSP00000509156.1:n.1264+51_1264+52del
ENST00000690543.1:c.1765+51_1765+52del	ENSP00000508831.1:n.1765+51_1765+52del
ENST00000690917.1:n.1992+51_1992+52del
ENST00000691361.1:n.684+51_684+52del
ENST00000692783.1:c.1774+51_1774+52del	ENSP00000508733.1:n.1774+51_1774+52del
ENST00000692991.1:n.1871+51_1871+52del
ENST00000288135.6:c.1774+51_1774+52del MANE Select	ENSP00000288135.6:n.1774+51_1774+52del
ENST00000288135.5:c.1774+51_1774+52del	ENSP00000288135.5:n.1774+51_1774+52del
ENST00000412167.6:c.1762+51_1762+52del	ENSP00000390987.2:n.1762+51_1762+52del
NM_000222.2:c.1774+51_1774+52del , LRG_307t1:c.1774+51_1774+52del	NP_000213.1:n.1774+51_1774+52del
NM_001093772.1:c.1762+51_1762+52del	NP_001087241.1:n.1762+51_1762+52del
XM_005265740.1:c.1777+51_1777+52del	XP_005265797.1:n.1777+51_1777+52del
XM_005265741.1:c.1777+51_1777+52del	XP_005265798.1:n.1777+51_1777+52del
XM_005265742.1:c.1765+51_1765+52del	XP_005265799.1:n.1765+51_1765+52del
XM_005265742.3:c.1765+51_1765+52del	XP_005265799.1:n.1765+51_1765+52del
XM_017008178.1:c.1774+51_1774+52del	XP_016863667.1:n.1774+51_1774+52del
XM_017008179.1:c.1765+51_1765+52del	XP_016863668.1:n.1765+51_1765+52del
XM_017008180.1:c.1762+51_1762+52del	XP_016863669.1:n.1762+51_1762+52del
NM_000222.3:c.1774+51_1774+52del MANE Select	NP_000213.1:n.1774+51_1774+52del
NM_001093772.2:c.1762+51_1762+52del	NP_001087241.1:n.1762+51_1762+52del
NM_001385284.1:c.1777+51_1777+52del	NP_001372213.1:n.1777+51_1777+52del
NM_001385285.1:c.1774+51_1774+52del	NP_001372214.1:n.1774+51_1774+52del
NM_001385286.1:c.1762+51_1762+52del	NP_001372215.1:n.1762+51_1762+52del
NM_001385288.1:c.1765+51_1765+52del	NP_001372217.1:n.1765+51_1765+52del
NM_001385290.1:c.1777+51_1777+52del	NP_001372219.1:n.1777+51_1777+52del
NM_001385292.1:c.1765+51_1765+52del	NP_001372221.1:n.1765+51_1765+52del