Canonical Allele Identifier: CA386123001

Gene: KITLG

Linked Data

• MyVariant Identifiers: chr12:g.88939560A>C (hg19) ; chr12:g.88545783A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88545783A>C , CM000674.2:g.88545783A>C	GRCh38
NC_000012.11:g.88939560A>C , CM000674.1:g.88939560A>C	GRCh37
NC_000012.10:g.87463691A>C	NCBI36
NG_012098.1:g.39679T>G
NG_012098.2:g.39679T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000347404.10:c.98T>G	ENSP00000054216.5:p.Val33Gly
ENST00000644744.1:c.98T>G MANE Select	ENSP00000495951.1:p.Val33Gly
ENST00000646633.1:c.*99T>G	ENSP00000494139.1:n.*99T>G
ENST00000228280.9:c.98T>G	ENSP00000228280.5:p.Val33Gly
ENST00000347404.9:c.98T>G	ENSP00000054216.5:p.Val33Gly
ENST00000357116.4:c.-48+34481T>G	ENSP00000474021.1:n.-48+34481T>G
ENST00000552044.1:c.-56T>G	ENSP00000475042.1:n.-56T>G
NM_000899.4:c.98T>G	NP_000890.1:p.Val33Gly
NM_003994.5:c.98T>G	NP_003985.2:p.Val33Gly
NM_000899.5:c.98T>G MANE Select	NP_000890.1:p.Val33Gly
NM_003994.6:c.98T>G	NP_003985.2:p.Val33Gly