Canonical Allele Identifier: CA693135324

Gene: KITLG

Linked Data

• dbSNP Id: rs1277149804
• gnomAD v3: 12-88565763-C-A
• gnomAD v4: 12-88565763-C-A
• MyVariant Identifiers: chr12:g.88959540C>A (hg19) ; chr12:g.88565763C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88565763C>A , CM000674.2:g.88565763C>A	GRCh38
NC_000012.11:g.88959540C>A , CM000674.1:g.88959540C>A	GRCh37
NC_000012.10:g.87483671C>A	NCBI36
NG_012098.1:g.19699G>T
NG_012098.2:g.19699G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000347404.10:c.15+14501G>T	ENSP00000054216.5:n.15+14501G>T
ENST00000644744.1:c.15+14501G>T MANE Select	ENSP00000495951.1:n.15+14501G>T
ENST00000646633.1:c.*16+14326G>T	ENSP00000494139.1:n.*16+14326G>T
ENST00000228280.9:c.15+14501G>T	ENSP00000228280.5:n.15+14501G>T
ENST00000347404.9:c.15+14501G>T	ENSP00000054216.5:n.15+14501G>T
ENST00000357116.4:c.-48+14501G>T	ENSP00000474021.1:n.-48+14501G>T
ENST00000552044.1:c.-275-1419G>T	ENSP00000475042.1:n.-275-1419G>T
NM_000899.4:c.15+14501G>T	NP_000890.1:n.15+14501G>T
NM_003994.5:c.15+14501G>T	NP_003985.2:n.15+14501G>T
NM_000899.5:c.15+14501G>T MANE Select	NP_000890.1:n.15+14501G>T
NM_003994.6:c.15+14501G>T	NP_003985.2:n.15+14501G>T