Canonical Allele Identifier: CA2260087078
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586856C= , CM000679.2:g.41586856C= GRCh38
NC_000017.10:g.39743108C= , CM000679.1:g.39743108C= GRCh37
NC_000017.9:g.36996634C= NCBI36
NG_008624.1:g.5040G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.-22G= MANE Select ENSP00000167586.6:n.-22G=
ENST00000167586.6:c.-22G= ENSP00000167586.6:n.-22G=
NM_000526.4:c.-22G= NP_000517.2:n.-22G=
NM_000526.5:c.-22G= MANE Select NP_000517.3:n.-22G=