Canonical Allele Identifier: CA950257808

Gene: KITLG

Linked Data

• gnomAD v3: 12-88532280-AGGGGG-A
• gnomAD v4: 12-88532280-AGGGGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88532281_88532285del , CM000674.2:g.88532281_88532285del	GRCh38
NC_000012.11:g.88926058_88926062del , CM000674.1:g.88926058_88926062del	GRCh37
NC_000012.10:g.87450189_87450193del	NCBI36
NG_012098.1:g.53177_53181del
NG_012098.2:g.53177_53181del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347404.10:c.192+156_192+160del	ENSP00000054216.5:n.192+156_192+160del
ENST00000644744.1:c.192+156_192+160del MANE Select	ENSP00000495951.1:n.192+156_192+160del
ENST00000646633.1:c.*193+156_*193+160del	ENSP00000494139.1:n.*193+156_*193+160del
ENST00000228280.9:c.192+156_192+160del	ENSP00000228280.5:n.192+156_192+160del
ENST00000347404.9:c.192+156_192+160del	ENSP00000054216.5:n.192+156_192+160del
ENST00000357116.4:c.-47-25148_-47-25144del	ENSP00000474021.1:n.-47-25148_-47-25144del
ENST00000378535.4:n.135+156_135+160del
ENST00000552044.1:c.39+156_39+160del	ENSP00000475042.1:n.39+156_39+160del
NM_000899.4:c.192+156_192+160del	NP_000890.1:n.192+156_192+160del
NM_003994.5:c.192+156_192+160del	NP_003985.2:n.192+156_192+160del
NM_000899.5:c.192+156_192+160del MANE Select	NP_000890.1:n.192+156_192+160del
NM_003994.6:c.192+156_192+160del	NP_003985.2:n.192+156_192+160del