Canonical Allele Identifier: CA2531306260
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036434_33036437del , CM000675.2:g.33036434_33036437del GRCh38
NC_000013.10:g.33610571_33610574del , CM000675.1:g.33610571_33610574del GRCh37
NC_000013.9:g.32508571_32508574del NCBI36
NG_011485.1:g.25001_25004del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.820-17333_820-17330del MANE Select ENSP00000369442.3:n.820-17333_820-17330del
ENST00000380099.3:c.820-17333_820-17330del ENSP00000369442.3:n.820-17333_820-17330del
ENST00000487852.1:n.828-17333_828-17330del
NM_004795.3:c.820-17333_820-17330del NP_004786.2:n.820-17333_820-17330del
XM_006719895.1:c.-102-17333_-102-17330del XP_006719958.1:n.-102-17333_-102-17330del
XM_006719895.2:c.-102-17333_-102-17330del XP_006719958.1:n.-102-17333_-102-17330del
NM_004795.4:c.820-17333_820-17330del MANE Select NP_004786.2:n.820-17333_820-17330del