Canonical Allele Identifier: CA290665533
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs111863334
MyVariant Identifiers: chr17:g.39742561C>G (hg19) chr17:g.41586309C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586309C>G , CM000679.2:g.41586309C>G GRCh38
NC_000017.10:g.39742561C>G , CM000679.1:g.39742561C>G GRCh37
NC_000017.9:g.36996087C>G NCBI36
NG_008624.1:g.5587G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.525+1G>C MANE Select ENSP00000167586.6:n.525+1G>C
ENST00000167586.6:c.525+1G>C ENSP00000167586.6:n.525+1G>C
NM_000526.4:c.525+1G>C NP_000517.2:n.525+1G>C
NM_000526.5:c.525+1G>C MANE Select NP_000517.3:n.525+1G>C
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