Canonical Allele Identifier: CA609106302

Gene: KL

Linked Data

• dbSNP Id: rs1469292134
• gnomAD v2: 13-33610471-AACACATGCACACACACCACACACACATACACATACCACATACATACCAC-A
• gnomAD v3: 13-33036334-AACACATGCACACACACCACACACACATACACATACCACATACATACCAC-A
• gnomAD v4: 13-33036334-AACACATGCACACACACCACACACACATACACATACCACATACATACCAC-A
• MyVariant Identifiers: chr13:g.33610472_33610520del (hg19) ; chr13:g.33036335_33036383del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33036361_33036409del , CM000675.2:g.33036361_33036409del	GRCh38
NC_000013.10:g.33610498_33610546del , CM000675.1:g.33610498_33610546del	GRCh37
NC_000013.9:g.32508498_32508546del	NCBI36
NG_011485.1:g.24928_24976del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.820-17406_820-17358del MANE Select	ENSP00000369442.3:n.820-17406_820-17358del
ENST00000380099.3:c.820-17406_820-17358del	ENSP00000369442.3:n.820-17406_820-17358del
ENST00000487852.1:n.828-17406_828-17358del
NM_004795.3:c.820-17406_820-17358del	NP_004786.2:n.820-17406_820-17358del
XM_006719895.1:c.-102-17406_-102-17358del	XP_006719958.1:n.-102-17406_-102-17358del
XM_006719895.2:c.-102-17406_-102-17358del	XP_006719958.1:n.-102-17406_-102-17358del
NM_004795.4:c.820-17406_820-17358del MANE Select	NP_004786.2:n.820-17406_820-17358del