Canonical Allele Identifier: CA2260099736
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs1908234517
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612383_41612394del , CM000679.2:g.41612383_41612394del GRCh38
NC_000017.10:g.39768635_39768646del , CM000679.1:g.39768635_39768646del GRCh37
NC_000017.9:g.37022161_37022172del NCBI36
NG_008301.1:g.5438_5449del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.299_310del MANE Select ENSP00000301653.3:p.Ala100_Gly103del
ENST00000301653.8:c.299_310del ENSP00000301653.3:p.Ala100_Gly103del
ENST00000588319.1:n.376_387del
ENST00000593067.1:c.-312-104_-312-93del ENSP00000467124.1:n.-312-104_-312-93del
NM_005557.3:c.299_310del NP_005548.2:p.Ala100_Gly103del
NM_005557.4:c.299_310del MANE Select NP_005548.2:p.Ala100_Gly103del
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Search 100 bp 3'