Canonical Allele Identifier: CA2260085927
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584410A= , CM000679.2:g.41584410A= GRCh38
NC_000017.10:g.39740662A= , CM000679.1:g.39740662A= GRCh37
NC_000017.9:g.36994188A= NCBI36
NG_008624.1:g.7486T=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.612T= MANE Select ENSP00000167586.6:p.Tyr204=
ENST00000167586.6:c.612T= ENSP00000167586.6:p.Tyr204=
ENST00000476662.1:n.62T=
NM_000526.4:c.612T= NP_000517.2:p.Tyr204=
NM_000526.5:c.612T= MANE Select NP_000517.3:p.Tyr204=