Canonical Allele Identifier: CA954749507
Gene: KL HGNC NCBI

Linked Data

dbSNP Id: rs1871132908
gnomAD v3: 13-33035861-ATAAAT-A
gnomAD v4: 13-33035861-ATAAAT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33035865_33035869del , CM000675.2:g.33035865_33035869del GRCh38
NC_000013.10:g.33610002_33610006del , CM000675.1:g.33610002_33610006del GRCh37
NC_000013.9:g.32508002_32508006del NCBI36
NG_011485.1:g.24432_24436del

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.820-17902_820-17898del MANE Select ENSP00000369442.3:n.820-17902_820-17898del
ENST00000380099.3:c.820-17902_820-17898del ENSP00000369442.3:n.820-17902_820-17898del
ENST00000487852.1:n.828-17902_828-17898del
NM_004795.3:c.820-17902_820-17898del NP_004786.2:n.820-17902_820-17898del
XM_006719895.1:c.-102-17902_-102-17898del XP_006719958.1:n.-102-17902_-102-17898del
XM_006719895.2:c.-102-17902_-102-17898del XP_006719958.1:n.-102-17902_-102-17898del
NM_004795.4:c.820-17902_820-17898del MANE Select NP_004786.2:n.820-17902_820-17898del
Search 100 bp 5'
Search 100 bp 3'