Canonical Allele Identifier: CA2260085601
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583872A= , CM000679.2:g.41583872A= GRCh38
NC_000017.10:g.39740124A= , CM000679.1:g.39740124A= GRCh37
NC_000017.9:g.36993650A= NCBI36
NG_008624.1:g.8024T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.815T= MANE Select ENSP00000167586.6:p.Met272=
ENST00000167586.6:c.815T= ENSP00000167586.6:p.Met272=
ENST00000476662.1:n.265T=
NM_000526.4:c.815T= NP_000517.2:p.Met272=
NM_000526.5:c.815T= MANE Select NP_000517.3:p.Met272=
Search 100 bp 5'
Search 100 bp 3'