Canonical Allele Identifier: CA399476943
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583672T>G , CM000679.2:g.41583672T>G GRCh38
NC_000017.10:g.39739924T>G , CM000679.1:g.39739924T>G GRCh37
NC_000017.9:g.36993450T>G NCBI36
NG_008624.1:g.8224A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.932A>C MANE Select ENSP00000167586.6:p.Glu311Ala
ENST00000167586.6:c.932A>C ENSP00000167586.6:p.Glu311Ala
ENST00000476662.1:n.382A>C
NM_000526.4:c.932A>C NP_000517.2:p.Glu311Ala
NM_000526.5:c.932A>C MANE Select NP_000517.3:p.Glu311Ala