Canonical Allele Identifier: CA2083142717
Gene: KL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33035936_33035937delinsTA , CM000675.2:g.33035936_33035937delinsTA GRCh38
NC_000013.10:g.33610073_33610074delinsTA , CM000675.1:g.33610073_33610074delinsTA GRCh37
NC_000013.9:g.32508073_32508074delinsTA NCBI36
NG_011485.1:g.24503_24504delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.820-17831_820-17830delinsTA MANE Select ENSP00000369442.3:n.820-17831_820-17830de...
ENST00000380099.3:c.820-17831_820-17830delinsTA ENSP00000369442.3:n.820-17831_820-17830de...
ENST00000487852.1:n.828-17831_828-17830delinsTA
NM_004795.3:c.820-17831_820-17830delinsTA NP_004786.2:n.820-17831_820-17830delinsTA...
XM_006719895.1:c.-102-17831_-102-17830delinsTA XP_006719958.1:n.-102-17831_-102-17830del...
XM_006719895.2:c.-102-17831_-102-17830delinsTA XP_006719958.1:n.-102-17831_-102-17830del...
NM_004795.4:c.820-17831_820-17830delinsTA MANE Select NP_004786.2:n.820-17831_820-17830delinsTA...