Canonical Allele Identifier: CA399481836
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39742592G>T (hg19) chr17:g.41586340G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586340G>T , CM000679.2:g.41586340G>T GRCh38
NC_000017.10:g.39742592G>T , CM000679.1:g.39742592G>T GRCh37
NC_000017.9:g.36996118G>T NCBI36
NG_008624.1:g.5556C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.495C>A MANE Select ENSP00000167586.6:p.Tyr165Ter
ENST00000167586.6:c.495C>A ENSP00000167586.6:p.Tyr165Ter
NM_000526.4:c.495C>A NP_000517.2:p.Tyr165Ter
NM_000526.5:c.495C>A MANE Select NP_000517.3:p.Tyr165Ter
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