Canonical Allele Identifier: CA2260085471
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583593G= , CM000679.2:g.41583593G= GRCh38
NC_000017.10:g.39739845G= , CM000679.1:g.39739845G= GRCh37
NC_000017.9:g.36993371G= NCBI36
NG_008624.1:g.8303C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1011C= MANE Select ENSP00000167586.6:p.Thr337=
ENST00000167586.6:c.1011C= ENSP00000167586.6:p.Thr337=
ENST00000476662.1:n.461C=
NM_000526.4:c.1011C= NP_000517.2:p.Thr337=
NM_000526.5:c.1011C= MANE Select NP_000517.3:p.Thr337=