Canonical Allele Identifier: CA8562599
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs760721828
ExAC: 17:39740111 AG / A
gnomAD v2: 17-39740111-AG-A
gnomAD v3: 17-41583859-AG-A
gnomAD v4: 17-41583859-AG-A
MyVariant Identifiers: chr17:g.39740112del (hg19) chr17:g.41583860del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583861del , CM000679.2:g.41583861del GRCh38
NC_000017.10:g.39740113del , CM000679.1:g.39740113del GRCh37
NC_000017.9:g.36993639del NCBI36
NG_008624.1:g.8036del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.827del MANE Select ENSP00000167586.6:p.Pro276LeufsTer5
ENST00000167586.6:c.827del ENSP00000167586.6:p.Pro276LeufsTer5
ENST00000476662.1:n.277del
NM_000526.4:c.827del NP_000517.2:p.Pro276LeufsTer5
NM_000526.5:c.827del MANE Select NP_000517.3:p.Pro276LeufsTer5
Search 100 bp 5'
Search 100 bp 3'