Canonical Allele Identifier: CA2053129483
Gene: KITLG HGNC NCBI

Linked Data

dbSNP Id: rs1871250169

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88560153T>C , CM000674.2:g.88560153T>C GRCh38
NC_000012.11:g.88953930T>C , CM000674.1:g.88953930T>C GRCh37
NC_000012.10:g.87478061T>C NCBI36
NG_012098.1:g.25309A>G
NG_012098.2:g.25309A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000347404.10:c.16-14288A>G ENSP00000054216.5:n.16-14288A>G
ENST00000644744.1:c.16-14288A>G MANE Select ENSP00000495951.1:n.16-14288A>G
ENST00000646633.1:c.*17-14288A>G ENSP00000494139.1:n.*17-14288A>G
ENST00000228280.9:c.16-14288A>G ENSP00000228280.5:n.16-14288A>G
ENST00000347404.9:c.16-14288A>G ENSP00000054216.5:n.16-14288A>G
ENST00000357116.4:c.-48+20111A>G ENSP00000474021.1:n.-48+20111A>G
ENST00000552044.1:c.-139+4055A>G ENSP00000475042.1:n.-139+4055A>G
NM_000899.4:c.16-14288A>G NP_000890.1:n.16-14288A>G
NM_003994.5:c.16-14288A>G NP_003985.2:n.16-14288A>G
NM_000899.5:c.16-14288A>G MANE Select NP_000890.1:n.16-14288A>G
NM_003994.6:c.16-14288A>G NP_003985.2:n.16-14288A>G