Canonical Allele Identifier: CA950257818

Gene: KITLG

Linked Data

• gnomAD v3: 12-88532285-G-GAAAAA
• gnomAD v4: 12-88532285-G-GAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88532289_88532293dup , CM000674.2:g.88532289_88532293dup	GRCh38
NC_000012.11:g.88926066_88926070dup , CM000674.1:g.88926066_88926070dup	GRCh37
NC_000012.10:g.87450197_87450201dup	NCBI36
NG_012098.1:g.53172_53176dup
NG_012098.2:g.53172_53176dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347404.10:c.192+151_192+155dup	ENSP00000054216.5:n.192+151_192+155dup
ENST00000644744.1:c.192+151_192+155dup MANE Select	ENSP00000495951.1:n.192+151_192+155dup
ENST00000646633.1:c.*193+151_*193+155dup	ENSP00000494139.1:n.*193+151_*193+155dup
ENST00000228280.9:c.192+151_192+155dup	ENSP00000228280.5:n.192+151_192+155dup
ENST00000347404.9:c.192+151_192+155dup	ENSP00000054216.5:n.192+151_192+155dup
ENST00000357116.4:c.-47-25153_-47-25149dup	ENSP00000474021.1:n.-47-25153_-47-25149dup
ENST00000378535.4:n.135+151_135+155dup
ENST00000552044.1:c.39+151_39+155dup	ENSP00000475042.1:n.39+151_39+155dup
NM_000899.4:c.192+151_192+155dup	NP_000890.1:n.192+151_192+155dup
NM_003994.5:c.192+151_192+155dup	NP_003985.2:n.192+151_192+155dup
NM_000899.5:c.192+151_192+155dup MANE Select	NP_000890.1:n.192+151_192+155dup
NM_003994.6:c.192+151_192+155dup	NP_003985.2:n.192+151_192+155dup