Canonical Allele Identifier: CA8562560
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs763362842

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583673C>T , CM000679.2:g.41583673C>T GRCh38
NC_000017.10:g.39739925C>T , CM000679.1:g.39739925C>T GRCh37
NC_000017.9:g.36993451C>T NCBI36
NG_008624.1:g.8223G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.931G>A MANE Select ENSP00000167586.6:p.Glu311Lys
ENST00000167586.6:c.931G>A ENSP00000167586.6:p.Glu311Lys
ENST00000476662.1:n.381G>A
NM_000526.4:c.931G>A NP_000517.2:p.Glu311Lys
NM_000526.5:c.931G>A MANE Select NP_000517.3:p.Glu311Lys