Canonical Allele Identifier: CA13672259
Gene: KITLG HGNC NCBI

Linked Data

dbSNP Id: rs3782179

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88559549C>T , CM000674.2:g.88559549C>T GRCh38
NC_000012.11:g.88953326C>T , CM000674.1:g.88953326C>T GRCh37
NC_000012.10:g.87477457C>T NCBI36
NG_012098.1:g.25913G>A
NG_012098.2:g.25913G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000347404.10:c.16-13684G>A ENSP00000054216.5:p.=
ENST00000644744.1:c.16-13684G>A MANE Select ENSP00000495951.1:p.=
ENST00000646633.1:c.*17-13684G>A ENSP00000494139.1:p.=
ENST00000228280.9:c.16-13684G>A ENSP00000228280.5:p.=
ENST00000347404.9:c.16-13684G>A ENSP00000054216.5:p.=
ENST00000357116.4:c.-48+20715G>A ENSP00000474021.1:p.=
ENST00000552044.1:c.-139+4659G>A ENSP00000475042.1:p.=
NM_000899.4:c.16-13684G>A NP_000890.1:p.=
NM_003994.5:c.16-13684G>A NP_003985.2:p.=
NM_000899.5:c.16-13684G>A MANE Select NP_000890.1:p.=
NM_003994.6:c.16-13684G>A NP_003985.2:p.=