Canonical Allele Identifier: CA399475718
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39739595C>G (hg19) chr17:g.41583343C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583343C>G , CM000679.2:g.41583343C>G GRCh38
NC_000017.10:g.39739595C>G , CM000679.1:g.39739595C>G GRCh37
NC_000017.9:g.36993121C>G NCBI36
NG_008624.1:g.8553G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1166G>C MANE Select ENSP00000167586.6:p.Cys389Ser
ENST00000167586.6:c.1166G>C ENSP00000167586.6:p.Cys389Ser
ENST00000441550.2:n.113G>C
ENST00000476662.1:n.616G>C
NM_000526.4:c.1166G>C NP_000517.2:p.Cys389Ser
NM_000526.5:c.1166G>C MANE Select NP_000517.3:p.Cys389Ser
Search 100 bp 5'
Search 100 bp 3'