Canonical Allele Identifier: CA2260087021
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586761C= , CM000679.2:g.41586761C= GRCh38
NC_000017.10:g.39743013C= , CM000679.1:g.39743013C= GRCh37
NC_000017.9:g.36996539C= NCBI36
NG_008624.1:g.5135G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.74G= MANE Select ENSP00000167586.6:p.Gly25=
ENST00000167586.6:c.74G= ENSP00000167586.6:p.Gly25=
NM_000526.4:c.74G= NP_000517.2:p.Gly25=
NM_000526.5:c.74G= MANE Select NP_000517.3:p.Gly25=