Canonical Allele Identifier: CA290665235
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs769181084
MyVariant Identifiers: chr17:g.39740911C>G (hg19) chr17:g.41584659C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584659C>G , CM000679.2:g.41584659C>G GRCh38
NC_000017.10:g.39740911C>G , CM000679.1:g.39740911C>G GRCh37
NC_000017.9:g.36994437C>G NCBI36
NG_008624.1:g.7237G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.609-246G>C MANE Select ENSP00000167586.6:n.609-246G>C
ENST00000167586.6:c.609-246G>C ENSP00000167586.6:n.609-246G>C
NM_000526.4:c.609-246G>C NP_000517.2:n.609-246G>C
NM_000526.5:c.609-246G>C MANE Select NP_000517.3:n.609-246G>C
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