Canonical Allele Identifier: CA2053129189
Community Standard Title: NM_000899.5(KITLG):c.16-13684G=
Gene: KITLG HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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