Canonical Allele Identifier: CA2260086999
Gene: KRT14 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586727G= , CM000679.2:g.41586727G= GRCh38
NC_000017.10:g.39742979G= , CM000679.1:g.39742979G= GRCh37
NC_000017.9:g.36996505G= NCBI36
NG_008624.1:g.5169C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.108C= MANE Select ENSP00000167586.6:p.Ala36=
ENST00000167586.6:c.108C= ENSP00000167586.6:p.Ala36=
NM_000526.4:c.108C= NP_000517.2:p.Ala36=
NM_000526.5:c.108C= MANE Select NP_000517.3:p.Ala36=
Search 100 bp 5'
Search 100 bp 3'