Canonical Allele Identifier: CA2083143040
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036367_33036370delinsTACC , CM000675.2:g.33036367_33036370delinsTACC GRCh38
NC_000013.10:g.33610504_33610507delinsTACC , CM000675.1:g.33610504_33610507delinsTACC GRCh37
NC_000013.9:g.32508504_32508507delinsTACC NCBI36
NG_011485.1:g.24934_24937delinsTACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.820-17400_820-17397delinsTACC MANE Select ENSP00000369442.3:n.820-17400_820-17397delinsTACC
ENST00000380099.3:c.820-17400_820-17397delinsTACC ENSP00000369442.3:n.820-17400_820-17397delinsTACC
ENST00000487852.1:n.828-17400_828-17397delinsTACC
NM_004795.3:c.820-17400_820-17397delinsTACC NP_004786.2:n.820-17400_820-17397delinsTACC
XM_006719895.1:c.-102-17400_-102-17397delinsTACC XP_006719958.1:n.-102-17400_-102-17397delinsTACC
XM_006719895.2:c.-102-17400_-102-17397delinsTACC XP_006719958.1:n.-102-17400_-102-17397delinsTACC
NM_004795.4:c.820-17400_820-17397delinsTACC MANE Select NP_004786.2:n.820-17400_820-17397delinsTACC