Canonical Allele Identifier: CA2260086827
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586456C= , CM000679.2:g.41586456C= GRCh38
NC_000017.10:g.39742708C= , CM000679.1:g.39742708C= GRCh37
NC_000017.9:g.36996234C= NCBI36
NG_008624.1:g.5440G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.379G= MANE Select ENSP00000167586.6:p.Ala127=
ENST00000167586.6:c.379G= ENSP00000167586.6:p.Ala127=
NM_000526.4:c.379G= NP_000517.2:p.Ala127=
NM_000526.5:c.379G= MANE Select NP_000517.3:p.Ala127=