Canonical Allele Identifier: CA2083142927
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036221_33036224delinsTACG , CM000675.2:g.33036221_33036224delinsTACG GRCh38
NC_000013.10:g.33610358_33610361delinsTACG , CM000675.1:g.33610358_33610361delinsTACG GRCh37
NC_000013.9:g.32508358_32508361delinsTACG NCBI36
NG_011485.1:g.24788_24791delinsTACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.820-17546_820-17543delinsTACG MANE Select ENSP00000369442.3:n.820-17546_820-17543delinsTACG
ENST00000380099.3:c.820-17546_820-17543delinsTACG ENSP00000369442.3:n.820-17546_820-17543delinsTACG
ENST00000487852.1:n.828-17546_828-17543delinsTACG
NM_004795.3:c.820-17546_820-17543delinsTACG NP_004786.2:n.820-17546_820-17543delinsTACG
XM_006719895.1:c.-102-17546_-102-17543delinsTACG XP_006719958.1:n.-102-17546_-102-17543delinsTACG
XM_006719895.2:c.-102-17546_-102-17543delinsTACG XP_006719958.1:n.-102-17546_-102-17543delinsTACG
NM_004795.4:c.820-17546_820-17543delinsTACG MANE Select NP_004786.2:n.820-17546_820-17543delinsTACG