Canonical Allele Identifier: CA386122879
Gene: KITLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88532483G>C , CM000674.2:g.88532483G>C GRCh38
NC_000012.11:g.88926260G>C , CM000674.1:g.88926260G>C GRCh37
NC_000012.10:g.87450391G>C NCBI36
NG_012098.1:g.52979C>G
NG_012098.2:g.52979C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000347404.10:c.150C>G ENSP00000054216.5:p.Asp50Glu
ENST00000644744.1:c.150C>G MANE Select ENSP00000495951.1:p.Asp50Glu
ENST00000646633.1:c.*151C>G ENSP00000494139.1:n.*151C>G
ENST00000228280.9:c.150C>G ENSP00000228280.5:p.Asp50Glu
ENST00000347404.9:c.150C>G ENSP00000054216.5:p.Asp50Glu
ENST00000357116.4:c.-47-25346C>G ENSP00000474021.1:n.-47-25346C>G
ENST00000378535.4:n.93C>G
ENST00000552044.1:c.-4C>G ENSP00000475042.1:n.-4C>G
NM_000899.4:c.150C>G NP_000890.1:p.Asp50Glu
NM_003994.5:c.150C>G NP_003985.2:p.Asp50Glu
NM_000899.5:c.150C>G MANE Select NP_000890.1:p.Asp50Glu
NM_003994.6:c.150C>G NP_003985.2:p.Asp50Glu