Canonical Allele Identifier: CA2260099724
Gene: KRT16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612361_41612373delinsCACCACCAGCAAA , CM000679.2:g.41612361_41612373delinsCACCACCAGCAAA GRCh38
NC_000017.10:g.39768613_39768625delinsCACCACCAGCAAA , CM000679.1:g.39768613_39768625delinsCACCACCAGCAAA GRCh37
NC_000017.9:g.37022139_37022151delinsCACCACCAGCAAA NCBI36
NG_008301.1:g.5455_5467delinsTTTGCTGGTGGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.316_328delinsTTTGCTGGTGGTG MANE Select ENSP00000301653.3:p.Phe106=
ENST00000301653.8:c.316_328delinsTTTGCTGGTGGTG ENSP00000301653.3:p.Phe106=
ENST00000588319.1:n.393_405delinsTTTGCTGGTGGTG
ENST00000593067.1:c.-312-87_-312-75delinsTTTGCTGGTGGTG ENSP00000467124.1:n.-312-87_-312-75delinsTTTGCTGGTGGTG
NM_005557.3:c.316_328delinsTTTGCTGGTGGTG NP_005548.2:p.Phe106=
NM_005557.4:c.316_328delinsTTTGCTGGTGGTG MANE Select NP_005548.2:p.Phe106=
Search 100 bp 5'
Search 100 bp 3'