Canonical Allele Identifier: CA2260085335
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583299C= , CM000679.2:g.41583299C= GRCh38
NC_000017.10:g.39739551C= , CM000679.1:g.39739551C= GRCh37
NC_000017.9:g.36993077C= NCBI36
NG_008624.1:g.8597G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1210G= MANE Select ENSP00000167586.6:p.Val404=
ENST00000167586.6:c.1210G= ENSP00000167586.6:p.Val404=
ENST00000441550.2:n.157G=
ENST00000476662.1:n.660G=
NM_000526.4:c.1210G= NP_000517.2:p.Val404=
NM_000526.5:c.1210G= MANE Select NP_000517.3:p.Val404=