Canonical Allele Identifier: CA2260085542
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583727G= , CM000679.2:g.41583727G= GRCh38
NC_000017.10:g.39739979G= , CM000679.1:g.39739979G= GRCh37
NC_000017.9:g.36993505G= NCBI36
NG_008624.1:g.8169C=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.927+33C= MANE Select ENSP00000167586.6:n.927+33C=
ENST00000167586.6:c.927+33C= ENSP00000167586.6:n.927+33C=
ENST00000476662.1:n.377+33C=
NM_000526.4:c.927+33C= NP_000517.2:n.927+33C=
NM_000526.5:c.927+33C= MANE Select NP_000517.3:n.927+33C=