Canonical Allele Identifier: CA2083142777
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036025_33036032delinsTAAGTAAC , CM000675.2:g.33036025_33036032delinsTAAGTAAC GRCh38
NC_000013.10:g.33610162_33610169delinsTAAGTAAC , CM000675.1:g.33610162_33610169delinsTAAGTAAC GRCh37
NC_000013.9:g.32508162_32508169delinsTAAGTAAC NCBI36
NG_011485.1:g.24592_24599delinsTAAGTAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.820-17742_820-17735delinsTAAGTAAC MANE Select ENSP00000369442.3:n.820-17742_820-17735delinsTAAGTAAC
ENST00000380099.3:c.820-17742_820-17735delinsTAAGTAAC ENSP00000369442.3:n.820-17742_820-17735delinsTAAGTAAC
ENST00000487852.1:n.828-17742_828-17735delinsTAAGTAAC
NM_004795.3:c.820-17742_820-17735delinsTAAGTAAC NP_004786.2:n.820-17742_820-17735delinsTAAGTAAC
XM_006719895.1:c.-102-17742_-102-17735delinsTAAGTAAC XP_006719958.1:n.-102-17742_-102-17735delinsTAAGTAAC
XM_006719895.2:c.-102-17742_-102-17735delinsTAAGTAAC XP_006719958.1:n.-102-17742_-102-17735delinsTAAGTAAC
NM_004795.4:c.820-17742_820-17735delinsTAAGTAAC MANE Select NP_004786.2:n.820-17742_820-17735delinsTAAGTAAC