Canonical Allele Identifier: CA2083142710
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33035930_33035931delinsCT , CM000675.2:g.33035930_33035931delinsCT GRCh38
NC_000013.10:g.33610067_33610068delinsCT , CM000675.1:g.33610067_33610068delinsCT GRCh37
NC_000013.9:g.32508067_32508068delinsCT NCBI36
NG_011485.1:g.24497_24498delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.820-17837_820-17836delinsCT MANE Select ENSP00000369442.3:n.820-17837_820-17836de...
ENST00000380099.3:c.820-17837_820-17836delinsCT ENSP00000369442.3:n.820-17837_820-17836de...
ENST00000487852.1:n.828-17837_828-17836delinsCT
NM_004795.3:c.820-17837_820-17836delinsCT NP_004786.2:n.820-17837_820-17836delinsCT...
XM_006719895.1:c.-102-17837_-102-17836delinsCT XP_006719958.1:n.-102-17837_-102-17836del...
XM_006719895.2:c.-102-17837_-102-17836delinsCT XP_006719958.1:n.-102-17837_-102-17836del...
NM_004795.4:c.820-17837_820-17836delinsCT MANE Select NP_004786.2:n.820-17837_820-17836delinsCT...