Canonical Allele Identifier: CA2620119559

Gene: KITLG

Linked Data

• gnomAD v4: 12-88532513-CAAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88532522_88532524del , CM000674.2:g.88532522_88532524del	GRCh38
NC_000012.11:g.88926299_88926301del , CM000674.1:g.88926299_88926301del	GRCh37
NC_000012.10:g.87450430_87450432del	NCBI36
NG_012098.1:g.52946_52948del
NG_012098.2:g.52946_52948del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347404.10:c.130-13_130-11del	ENSP00000054216.5:n.130-13_130-11del
ENST00000644744.1:c.130-13_130-11del MANE Select	ENSP00000495951.1:n.130-13_130-11del
ENST00000646633.1:c.*131-13_*131-11del	ENSP00000494139.1:n.*131-13_*131-11del
ENST00000228280.9:c.130-13_130-11del	ENSP00000228280.5:n.130-13_130-11del
ENST00000347404.9:c.130-13_130-11del	ENSP00000054216.5:n.130-13_130-11del
ENST00000357116.4:c.-47-25379_-47-25377del	ENSP00000474021.1:n.-47-25379_-47-25377del
ENST00000378535.4:n.73-13_73-11del
ENST00000552044.1:c.-24-13_-24-11del	ENSP00000475042.1:n.-24-13_-24-11del
NM_000899.4:c.130-13_130-11del	NP_000890.1:n.130-13_130-11del
NM_003994.5:c.130-13_130-11del	NP_003985.2:n.130-13_130-11del
NM_000899.5:c.130-13_130-11del MANE Select	NP_000890.1:n.130-13_130-11del
NM_003994.6:c.130-13_130-11del	NP_003985.2:n.130-13_130-11del