Canonical Allele Identifier: CA8562794
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs746280783
ExAC: 17:39742900 A / ATT
MyVariant Identifiers: chr17:g.39742900_39742901insTT (hg19) chr17:g.41586648_41586649insTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586648_41586649insTT , CM000679.2:g.41586648_41586649insTT GRCh38
NC_000017.10:g.39742900_39742901insTT , CM000679.1:g.39742900_39742901insTT GRCh37
NC_000017.9:g.36996426_36996427insTT NCBI36
NG_008624.1:g.5247_5248insAA

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.186_187insAA MANE Select ENSP00000167586.6:p.Cys63AsnfsTer?
ENST00000167586.6:c.186_187insAA ENSP00000167586.6:p.Cys63AsnfsTer?
NM_000526.4:c.186_187insAA NP_000517.2:p.Tyr63AsnfsTer?
NM_000526.5:c.186_187insAA MANE Select NP_000517.3:p.Cys63AsnfsTer?
Search 100 bp 5'
Search 100 bp 3'