Canonical Allele Identifier: CA2260099744
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs1908235254
gnomAD v4: 17-41612383-AAAGCCAGCACCC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612390_41612401del , CM000679.2:g.41612390_41612401del GRCh38
NC_000017.10:g.39768642_39768653del , CM000679.1:g.39768642_39768653del GRCh37
NC_000017.9:g.37022168_37022179del NCBI36
NG_008301.1:g.5433_5444del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.294_305del MANE Select ENSP00000301653.3:p.Leu98_Gly101del
ENST00000301653.8:c.294_305del ENSP00000301653.3:p.Leu98_Gly101del
ENST00000588319.1:n.371_382del
ENST00000593067.1:c.-312-109_-312-98del ENSP00000467124.1:n.-312-109_-312-98del
NM_005557.3:c.294_305del NP_005548.2:p.Leu98_Gly101del
NM_005557.4:c.294_305del MANE Select NP_005548.2:p.Leu98_Gly101del
Search 100 bp 5'
Search 100 bp 3'