Canonical Allele Identifier: CA2260085524
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583695C= , CM000679.2:g.41583695C= GRCh38
NC_000017.10:g.39739947C= , CM000679.1:g.39739947C= GRCh37
NC_000017.9:g.36993473C= NCBI36
NG_008624.1:g.8201G=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.928-19G= MANE Select ENSP00000167586.6:n.928-19G=
ENST00000167586.6:c.928-19G= ENSP00000167586.6:n.928-19G=
ENST00000476662.1:n.378-19G=
NM_000526.4:c.928-19G= NP_000517.2:n.928-19G=
NM_000526.5:c.928-19G= MANE Select NP_000517.3:n.928-19G=