Canonical Allele Identifier: CA2260085268
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583197C= , CM000679.2:g.41583197C= GRCh38
NC_000017.10:g.39739449C= , CM000679.1:g.39739449C= GRCh37
NC_000017.9:g.36992975C= NCBI36
NG_008624.1:g.8699G=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1274+38G= MANE Select ENSP00000167586.6:n.1274+38G=
ENST00000167586.6:c.1274+38G= ENSP00000167586.6:n.1274+38G=
ENST00000441550.2:n.221+38G=
NM_000526.4:c.1274+38G= NP_000517.2:n.1274+38G=
NM_000526.5:c.1274+38G= MANE Select NP_000517.3:n.1274+38G=