Canonical Allele Identifier: CA6713778

Gene: KITLG

Linked Data

• dbSNP Id: rs778387015
• ExAC: 12:88926301 AT / A
• gnomAD v2: 12-88926301-AT-A
• gnomAD v4: 12-88532524-AT-A
• MyVariant Identifiers: chr12:g.88926302del (hg19) ; chr12:g.88532525del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88532526del , CM000674.2:g.88532526del	GRCh38
NC_000012.11:g.88926303del , CM000674.1:g.88926303del	GRCh37
NC_000012.10:g.87450434del	NCBI36
NG_012098.1:g.52937del
NG_012098.2:g.52937del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347404.10:c.130-22del	ENSP00000054216.5:n.130-22del
ENST00000644744.1:c.130-22del MANE Select	ENSP00000495951.1:n.130-22del
ENST00000646633.1:c.*131-22del	ENSP00000494139.1:n.*131-22del
ENST00000228280.9:c.130-22del	ENSP00000228280.5:n.130-22del
ENST00000347404.9:c.130-22del	ENSP00000054216.5:n.130-22del
ENST00000357116.4:c.-47-25388del	ENSP00000474021.1:n.-47-25388del
ENST00000378535.4:n.73-22del
ENST00000552044.1:c.-24-22del	ENSP00000475042.1:n.-24-22del
NM_000899.4:c.130-22del	NP_000890.1:n.130-22del
NM_003994.5:c.130-22del	NP_003985.2:n.130-22del
NM_000899.5:c.130-22del MANE Select	NP_000890.1:n.130-22del
NM_003994.6:c.130-22del	NP_003985.2:n.130-22del