Canonical Allele Identifier: CA2053117149

Gene: KITLG

Linked Data

• dbSNP Id: rs1870122916

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88532217dup , CM000674.2:g.88532217dup	GRCh38
NC_000012.11:g.88925994dup , CM000674.1:g.88925994dup	GRCh37
NC_000012.10:g.87450125dup	NCBI36
NG_012098.1:g.53246dup
NG_012098.2:g.53246dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347404.10:c.192+225dup	ENSP00000054216.5:n.192+225dup
ENST00000644744.1:c.192+225dup MANE Select	ENSP00000495951.1:n.192+225dup
ENST00000646633.1:c.*193+225dup	ENSP00000494139.1:n.*193+225dup
ENST00000228280.9:c.192+225dup	ENSP00000228280.5:n.192+225dup
ENST00000347404.9:c.192+225dup	ENSP00000054216.5:n.192+225dup
ENST00000357116.4:c.-47-25079dup	ENSP00000474021.1:n.-47-25079dup
ENST00000378535.4:n.135+225dup
ENST00000552044.1:c.39+225dup	ENSP00000475042.1:n.39+225dup
NM_000899.4:c.192+225dup	NP_000890.1:n.192+225dup
NM_003994.5:c.192+225dup	NP_003985.2:n.192+225dup
NM_000899.5:c.192+225dup MANE Select	NP_000890.1:n.192+225dup
NM_003994.6:c.192+225dup	NP_003985.2:n.192+225dup