Canonical Allele Identifier: CA2260085974
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584503T= , CM000679.2:g.41584503T= GRCh38
NC_000017.10:g.39740755T= , CM000679.1:g.39740755T= GRCh37
NC_000017.9:g.36994281T= NCBI36
NG_008624.1:g.7393A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.609-90A= MANE Select ENSP00000167586.6:n.609-90A=
ENST00000167586.6:c.609-90A= ENSP00000167586.6:n.609-90A=
NM_000526.4:c.609-90A= NP_000517.2:n.609-90A=
NM_000526.5:c.609-90A= MANE Select NP_000517.3:n.609-90A=