Canonical Allele Identifier: CA2083143090

Gene: KL

Linked Data

• dbSNP Id: rs1871148585

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33036411_33036413del , CM000675.2:g.33036411_33036413del	GRCh38
NC_000013.10:g.33610548_33610550del , CM000675.1:g.33610548_33610550del	GRCh37
NC_000013.9:g.32508548_32508550del	NCBI36
NG_011485.1:g.24978_24980del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.820-17356_820-17354del MANE Select	ENSP00000369442.3:n.820-17356_820-17354del
ENST00000380099.3:c.820-17356_820-17354del	ENSP00000369442.3:n.820-17356_820-17354del
ENST00000487852.1:n.828-17356_828-17354del
NM_004795.3:c.820-17356_820-17354del	NP_004786.2:n.820-17356_820-17354del
XM_006719895.1:c.-102-17356_-102-17354del	XP_006719958.1:n.-102-17356_-102-17354del
XM_006719895.2:c.-102-17356_-102-17354del	XP_006719958.1:n.-102-17356_-102-17354del
NM_004795.4:c.820-17356_820-17354del MANE Select	NP_004786.2:n.820-17356_820-17354del