Canonical Allele Identifier: CA2535826477

Gene: KITLG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88532235_88532240del , CM000674.2:g.88532235_88532240del	GRCh38
NC_000012.11:g.88926012_88926017del , CM000674.1:g.88926012_88926017del	GRCh37
NC_000012.10:g.87450143_87450148del	NCBI36
NG_012098.1:g.53223_53228del
NG_012098.2:g.53223_53228del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347404.10:c.192+202_192+207del	ENSP00000054216.5:n.192+202_192+207del
ENST00000644744.1:c.192+202_192+207del MANE Select	ENSP00000495951.1:n.192+202_192+207del
ENST00000646633.1:c.*193+202_*193+207del	ENSP00000494139.1:n.*193+202_*193+207del
ENST00000228280.9:c.192+202_192+207del	ENSP00000228280.5:n.192+202_192+207del
ENST00000347404.9:c.192+202_192+207del	ENSP00000054216.5:n.192+202_192+207del
ENST00000357116.4:c.-47-25102_-47-25097del	ENSP00000474021.1:n.-47-25102_-47-25097del
ENST00000378535.4:n.135+202_135+207del
ENST00000552044.1:c.39+202_39+207del	ENSP00000475042.1:n.39+202_39+207del
NM_000899.4:c.192+202_192+207del	NP_000890.1:n.192+202_192+207del
NM_003994.5:c.192+202_192+207del	NP_003985.2:n.192+202_192+207del
NM_000899.5:c.192+202_192+207del MANE Select	NP_000890.1:n.192+202_192+207del
NM_003994.6:c.192+202_192+207del	NP_003985.2:n.192+202_192+207del