Canonical Allele Identifier: CA399478946
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584411T>G , CM000679.2:g.41584411T>G GRCh38
NC_000017.10:g.39740663T>G , CM000679.1:g.39740663T>G GRCh37
NC_000017.9:g.36994189T>G NCBI36
NG_008624.1:g.7485A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.611A>C MANE Select ENSP00000167586.6:p.Tyr204Ser
ENST00000167586.6:c.611A>C ENSP00000167586.6:p.Tyr204Ser
ENST00000476662.1:n.61A>C
NM_000526.4:c.611A>C NP_000517.2:p.Tyr204Ser
NM_000526.5:c.611A>C MANE Select NP_000517.3:p.Tyr204Ser