Canonical Allele Identifier: CA2620120752
Gene: KITLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88545690A>T , CM000674.2:g.88545690A>T GRCh38
NC_000012.11:g.88939467A>T , CM000674.1:g.88939467A>T GRCh37
NC_000012.10:g.87463598A>T NCBI36
NG_012098.1:g.39772T>A
NG_012098.2:g.39772T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000347404.10:c.129+62T>A ENSP00000054216.5:n.129+62T>A
ENST00000644744.1:c.129+62T>A MANE Select ENSP00000495951.1:n.129+62T>A
ENST00000646633.1:c.*130+62T>A ENSP00000494139.1:n.*130+62T>A
ENST00000228280.9:c.129+62T>A ENSP00000228280.5:n.129+62T>A
ENST00000347404.9:c.129+62T>A ENSP00000054216.5:n.129+62T>A
ENST00000357116.4:c.-48+34574T>A ENSP00000474021.1:n.-48+34574T>A
ENST00000552044.1:c.-25+62T>A ENSP00000475042.1:n.-25+62T>A
NM_000899.4:c.129+62T>A NP_000890.1:n.129+62T>A
NM_003994.5:c.129+62T>A NP_003985.2:n.129+62T>A
NM_000899.5:c.129+62T>A MANE Select NP_000890.1:n.129+62T>A
NM_003994.6:c.129+62T>A NP_003985.2:n.129+62T>A