Canonical Allele Identifier: CA954749526
Gene: KL HGNC NCBI

Linked Data

gnomAD v3: 13-33036339-ATG-A
gnomAD v4: 13-33036339-ATG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036340_33036341del , CM000675.2:g.33036340_33036341del GRCh38
NC_000013.10:g.33610477_33610478del , CM000675.1:g.33610477_33610478del GRCh37
NC_000013.9:g.32508477_32508478del NCBI36
NG_011485.1:g.24907_24908del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.820-17427_820-17426del MANE Select ENSP00000369442.3:n.820-17427_820-17426del
ENST00000380099.3:c.820-17427_820-17426del ENSP00000369442.3:n.820-17427_820-17426del
ENST00000487852.1:n.828-17427_828-17426del
NM_004795.3:c.820-17427_820-17426del NP_004786.2:n.820-17427_820-17426del
XM_006719895.1:c.-102-17427_-102-17426del XP_006719958.1:n.-102-17427_-102-17426del
XM_006719895.2:c.-102-17427_-102-17426del XP_006719958.1:n.-102-17427_-102-17426del
NM_004795.4:c.820-17427_820-17426del MANE Select NP_004786.2:n.820-17427_820-17426del
Search 100 bp 5'
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