Canonical Allele Identifier: CA2260085284
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583210G= , CM000679.2:g.41583210G= GRCh38
NC_000017.10:g.39739462G= , CM000679.1:g.39739462G= GRCh37
NC_000017.9:g.36992988G= NCBI36
NG_008624.1:g.8686C=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1274+25C= MANE Select ENSP00000167586.6:n.1274+25C=
ENST00000167586.6:c.1274+25C= ENSP00000167586.6:n.1274+25C=
ENST00000441550.2:n.221+25C=
NM_000526.4:c.1274+25C= NP_000517.2:n.1274+25C=
NM_000526.5:c.1274+25C= MANE Select NP_000517.3:n.1274+25C=