Canonical Allele Identifier: CA2260085321
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583275T= , CM000679.2:g.41583275T= GRCh38
NC_000017.10:g.39739527T= , CM000679.1:g.39739527T= GRCh37
NC_000017.9:g.36993053T= NCBI36
NG_008624.1:g.8621A=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1234A= MANE Select ENSP00000167586.6:p.Ile412=
ENST00000167586.6:c.1234A= ENSP00000167586.6:p.Ile412=
ENST00000441550.2:n.181A=
ENST00000476662.1:n.684A=
NM_000526.4:c.1234A= NP_000517.2:p.Ile412=
NM_000526.5:c.1234A= MANE Select NP_000517.3:p.Ile412=