Canonical Allele Identifier: CA2260085607
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583886A= , CM000679.2:g.41583886A= GRCh38
NC_000017.10:g.39740138A= , CM000679.1:g.39740138A= GRCh37
NC_000017.9:g.36993664A= NCBI36
NG_008624.1:g.8010T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.801T= MANE Select ENSP00000167586.6:p.Asp267=
ENST00000167586.6:c.801T= ENSP00000167586.6:p.Asp267=
ENST00000476662.1:n.251T=
NM_000526.4:c.801T= NP_000517.2:p.Asp267=
NM_000526.5:c.801T= MANE Select NP_000517.3:p.Asp267=
Search 100 bp 5'
Search 100 bp 3'