Canonical Allele Identifier: CA386123016

Gene: KITLG

Linked Data

• MyVariant Identifiers: chr12:g.88939567T>A (hg19) ; chr12:g.88545790T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88545790T>A , CM000674.2:g.88545790T>A	GRCh38
NC_000012.11:g.88939567T>A , CM000674.1:g.88939567T>A	GRCh37
NC_000012.10:g.87463698T>A	NCBI36
NG_012098.1:g.39672A>T
NG_012098.2:g.39672A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000347404.10:c.91A>T	ENSP00000054216.5:p.Asn31Tyr
ENST00000644744.1:c.91A>T MANE Select	ENSP00000495951.1:p.Asn31Tyr
ENST00000646633.1:c.*92A>T	ENSP00000494139.1:n.*92A>T
ENST00000228280.9:c.91A>T	ENSP00000228280.5:p.Asn31Tyr
ENST00000347404.9:c.91A>T	ENSP00000054216.5:p.Asn31Tyr
ENST00000357116.4:c.-48+34474A>T	ENSP00000474021.1:n.-48+34474A>T
ENST00000552044.1:c.-63A>T	ENSP00000475042.1:n.-63A>T
NM_000899.4:c.91A>T	NP_000890.1:p.Asn31Tyr
NM_003994.5:c.91A>T	NP_003985.2:p.Asn31Tyr
NM_000899.5:c.91A>T MANE Select	NP_000890.1:p.Asn31Tyr
NM_003994.6:c.91A>T	NP_003985.2:p.Asn31Tyr