Canonical Allele Identifier: CA2620119631

Gene: KITLG

Linked Data

• gnomAD v4: 12-88532603-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88532603T>C , CM000674.2:g.88532603T>C	GRCh38
NC_000012.11:g.88926380T>C , CM000674.1:g.88926380T>C	GRCh37
NC_000012.10:g.87450511T>C	NCBI36
NG_012098.1:g.52859A>G
NG_012098.2:g.52859A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347404.10:c.130-100A>G	ENSP00000054216.5:n.130-100A>G
ENST00000644744.1:c.130-100A>G MANE Select	ENSP00000495951.1:n.130-100A>G
ENST00000646633.1:c.*131-100A>G	ENSP00000494139.1:n.*131-100A>G
ENST00000228280.9:c.130-100A>G	ENSP00000228280.5:n.130-100A>G
ENST00000347404.9:c.130-100A>G	ENSP00000054216.5:n.130-100A>G
ENST00000357116.4:c.-47-25466A>G	ENSP00000474021.1:n.-47-25466A>G
ENST00000378535.4:n.73-100A>G
ENST00000552044.1:c.-24-100A>G	ENSP00000475042.1:n.-24-100A>G
NM_000899.4:c.130-100A>G	NP_000890.1:n.130-100A>G
NM_003994.5:c.130-100A>G	NP_003985.2:n.130-100A>G
NM_000899.5:c.130-100A>G MANE Select	NP_000890.1:n.130-100A>G
NM_003994.6:c.130-100A>G	NP_003985.2:n.130-100A>G