Canonical Allele Identifier: CA2637838399
Gene: KRT16 HGNC NCBI

Linked Data

gnomAD v4: 17-41612671-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612672del , CM000679.2:g.41612672del GRCh38
NC_000017.10:g.39768924del , CM000679.1:g.39768924del GRCh37
NC_000017.9:g.37022450del NCBI36
NG_008301.1:g.5156del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.17del MANE Select ENSP00000301653.3:p.Arg6ProfsTer9
ENST00000301653.8:c.17del ENSP00000301653.3:p.Arg6ProfsTer9
ENST00000588319.1:n.94del
ENST00000590990.1:c.17del ENSP00000467105.1:p.Arg6ProfsTer9
ENST00000593067.1:c.-313+118del ENSP00000467124.1:n.-313+118del
NM_005557.3:c.17del NP_005548.2:p.Arg6ProfsTer9
NM_005557.4:c.17del MANE Select NP_005548.2:p.Arg6ProfsTer9
Search 100 bp 5'
Search 100 bp 3'