Canonical Allele Identifier: CA241516957

Gene: KITLG

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88550016T>A , CM000674.2:g.88550016T>A	GRCh38
NC_000012.11:g.88943793T>A , CM000674.1:g.88943793T>A	GRCh37
NC_000012.10:g.87467924T>A	NCBI36
NG_012098.1:g.35446A>T
NG_012098.2:g.35446A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347404.10:c.16-4151A>T	ENSP00000054216.5:n.16-4151A>T
ENST00000644744.1:c.16-4151A>T MANE Select	ENSP00000495951.1:n.16-4151A>T
ENST00000646633.1:c.*17-4151A>T	ENSP00000494139.1:n.*17-4151A>T
ENST00000228280.9:c.16-4151A>T	ENSP00000228280.5:n.16-4151A>T
ENST00000347404.9:c.16-4151A>T	ENSP00000054216.5:n.16-4151A>T
ENST00000357116.4:c.-48+30248A>T	ENSP00000474021.1:n.-48+30248A>T
ENST00000552044.1:c.-138-4151A>T	ENSP00000475042.1:n.-138-4151A>T
NM_000899.4:c.16-4151A>T	NP_000890.1:n.16-4151A>T
NM_003994.5:c.16-4151A>T	NP_003985.2:n.16-4151A>T
NM_000899.5:c.16-4151A>T MANE Select	NP_000890.1:n.16-4151A>T
NM_003994.6:c.16-4151A>T	NP_003985.2:n.16-4151A>T