Canonical Allele Identifier: CA2053129398
Gene: KITLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88559994A= , CM000674.2:g.88559994A= GRCh38
NC_000012.11:g.88953771A= , CM000674.1:g.88953771A= GRCh37
NC_000012.10:g.87477902A= NCBI36
NG_012098.1:g.25468T=
NG_012098.2:g.25468T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000347404.10:c.16-14129T= ENSP00000054216.5:n.16-14129T=
ENST00000644744.1:c.16-14129T= MANE Select ENSP00000495951.1:n.16-14129T=
ENST00000646633.1:c.*17-14129T= ENSP00000494139.1:n.*17-14129T=
ENST00000228280.9:c.16-14129T= ENSP00000228280.5:n.16-14129T=
ENST00000347404.9:c.16-14129T= ENSP00000054216.5:n.16-14129T=
ENST00000357116.4:c.-48+20270T= ENSP00000474021.1:n.-48+20270T=
ENST00000552044.1:c.-139+4214T= ENSP00000475042.1:n.-139+4214T=
NM_000899.4:c.16-14129T= NP_000890.1:n.16-14129T=
NM_003994.5:c.16-14129T= NP_003985.2:n.16-14129T=
NM_000899.5:c.16-14129T= MANE Select NP_000890.1:n.16-14129T=
NM_003994.6:c.16-14129T= NP_003985.2:n.16-14129T=