Canonical Allele Identifier: CA2083143104

Gene: KL

Linked Data

• dbSNP Id: rs1871149494

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33036425_33036426insCACT , CM000675.2:g.33036425_33036426insCACT	GRCh38
NC_000013.10:g.33610562_33610563insCACT , CM000675.1:g.33610562_33610563insCACT	GRCh37
NC_000013.9:g.32508562_32508563insCACT	NCBI36
NG_011485.1:g.24992_24993insCACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.820-17342_820-17341insCACT MANE Select	ENSP00000369442.3:n.820-17342_820-17341insCACT
ENST00000380099.3:c.820-17342_820-17341insCACT	ENSP00000369442.3:n.820-17342_820-17341insCACT
ENST00000487852.1:n.828-17342_828-17341insCACT
NM_004795.3:c.820-17342_820-17341insCACT	NP_004786.2:n.820-17342_820-17341insCACT
XM_006719895.1:c.-102-17342_-102-17341insCACT	XP_006719958.1:n.-102-17342_-102-17341insCACT
XM_006719895.2:c.-102-17342_-102-17341insCACT	XP_006719958.1:n.-102-17342_-102-17341insCACT
NM_004795.4:c.820-17342_820-17341insCACT MANE Select	NP_004786.2:n.820-17342_820-17341insCACT