Canonical Allele Identifier: CA2083143089
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036407_33036410delinsACAC , CM000675.2:g.33036407_33036410delinsACAC GRCh38
NC_000013.10:g.33610544_33610547delinsACAC , CM000675.1:g.33610544_33610547delinsACAC GRCh37
NC_000013.9:g.32508544_32508547delinsACAC NCBI36
NG_011485.1:g.24974_24977delinsACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.820-17360_820-17357delinsACAC MANE Select ENSP00000369442.3:n.820-17360_820-17357delinsACAC
ENST00000380099.3:c.820-17360_820-17357delinsACAC ENSP00000369442.3:n.820-17360_820-17357delinsACAC
ENST00000487852.1:n.828-17360_828-17357delinsACAC
NM_004795.3:c.820-17360_820-17357delinsACAC NP_004786.2:n.820-17360_820-17357delinsACAC
XM_006719895.1:c.-102-17360_-102-17357delinsACAC XP_006719958.1:n.-102-17360_-102-17357delinsACAC
XM_006719895.2:c.-102-17360_-102-17357delinsACAC XP_006719958.1:n.-102-17360_-102-17357delinsACAC
NM_004795.4:c.820-17360_820-17357delinsACAC MANE Select NP_004786.2:n.820-17360_820-17357delinsACAC