Canonical Allele Identifier: CA8563388
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs763207283
ExAC: 17:39768969 GC / G
gnomAD v2: 17-39768969-GC-G
gnomAD v4: 17-41612717-GC-G
MyVariant Identifiers: chr17:g.39768970del (hg19) chr17:g.41612718del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612718del , CM000679.2:g.41612718del GRCh38
NC_000017.10:g.39768970del , CM000679.1:g.39768970del GRCh37
NC_000017.9:g.37022496del NCBI36
NG_008301.1:g.5110del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-30del MANE Select ENSP00000301653.3:n.-30del
ENST00000301653.8:c.-30del ENSP00000301653.3:n.-30del
ENST00000588319.1:n.48del
ENST00000590990.1:c.-30del ENSP00000467105.1:n.-30del
ENST00000593067.1:c.-313+72del ENSP00000467124.1:n.-313+72del
NM_005557.3:c.-30del NP_005548.2:n.-30del
NM_005557.4:c.-30del MANE Select NP_005548.2:n.-30del
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