Canonical Allele Identifier: CA2620119576
Gene: KITLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88532529A>T , CM000674.2:g.88532529A>T GRCh38
NC_000012.11:g.88926306A>T , CM000674.1:g.88926306A>T GRCh37
NC_000012.10:g.87450437A>T NCBI36
NG_012098.1:g.52933T>A
NG_012098.2:g.52933T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000347404.10:c.130-26T>A ENSP00000054216.5:n.130-26T>A
ENST00000644744.1:c.130-26T>A MANE Select ENSP00000495951.1:n.130-26T>A
ENST00000646633.1:c.*131-26T>A ENSP00000494139.1:n.*131-26T>A
ENST00000228280.9:c.130-26T>A ENSP00000228280.5:n.130-26T>A
ENST00000347404.9:c.130-26T>A ENSP00000054216.5:n.130-26T>A
ENST00000357116.4:c.-47-25392T>A ENSP00000474021.1:n.-47-25392T>A
ENST00000378535.4:n.73-26T>A
ENST00000552044.1:c.-24-26T>A ENSP00000475042.1:n.-24-26T>A
NM_000899.4:c.130-26T>A NP_000890.1:n.130-26T>A
NM_003994.5:c.130-26T>A NP_003985.2:n.130-26T>A
NM_000899.5:c.130-26T>A MANE Select NP_000890.1:n.130-26T>A
NM_003994.6:c.130-26T>A NP_003985.2:n.130-26T>A