Canonical Allele Identifier: CA2580611816

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727468_54727696del , CM000666.2:g.54727468_54727696del	GRCh38
NC_000004.11:g.55593634_55593862del , CM000666.1:g.55593634_55593862del	GRCh37
NC_000004.10:g.55288391_55288619del	NCBI36
NG_007456.1:g.74474_74702del , LRG_307:g.74474_74702del

Transcript Alleles

HGVS	Amino-acid change
ENST00000412167.7:c.1691_1766-127del
ENST00000685269.1:n.1778_1853-127del
ENST00000686011.1:c.1688_1763-127del
ENST00000687109.1:c.1703_1778-127del
ENST00000687208.1:n.2115_2190-127del
ENST00000687246.1:c.1688_1763-127del
ENST00000687265.1:n.1858_1933-127del
ENST00000687295.1:c.1688_1763-127del
ENST00000689832.1:c.1703_1778-127del
ENST00000689994.1:c.1190_1265-127del
ENST00000690543.1:c.1691_1766-127del
ENST00000690917.1:n.1918_1993-127del
ENST00000691361.1:n.610_685-127del
ENST00000692783.1:c.1700_1775-127del
ENST00000692991.1:n.1797_1872-127del
ENST00000288135.6:c.1700_1775-127del
ENST00000288135.5:c.1700_1775-127del
ENST00000412167.6:c.1688_1763-127del
NM_000222.2:c.1700_1775-127del , LRG_307t1:c.1700_1775-127del
NM_001093772.1:c.1688_1763-127del
XM_005265740.1:c.1703_1778-127del
XM_005265741.1:c.1703_1778-127del
XM_005265742.1:c.1691_1766-127del
XM_005265742.3:c.1691_1766-127del
XM_017008178.1:c.1700_1775-127del
XM_017008179.1:c.1691_1766-127del
XM_017008180.1:c.1688_1763-127del
NM_000222.3:c.1700_1775-127del
NM_001093772.2:c.1688_1763-127del
NM_001385284.1:c.1703_1778-127del
NM_001385285.1:c.1700_1775-127del
NM_001385286.1:c.1688_1763-127del
NM_001385288.1:c.1691_1766-127del
NM_001385290.1:c.1703_1778-127del
NM_001385292.1:c.1691_1766-127del