Canonical Allele Identifier: CA2260086972
Gene: KRT14 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586691G= , CM000679.2:g.41586691G= GRCh38
NC_000017.10:g.39742943G= , CM000679.1:g.39742943G= GRCh37
NC_000017.9:g.36996469G= NCBI36
NG_008624.1:g.5205C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.144C= MANE Select ENSP00000167586.6:p.Gly48=
ENST00000167586.6:c.144C= ENSP00000167586.6:p.Gly48=
NM_000526.4:c.144C= NP_000517.2:p.Gly48=
NM_000526.5:c.144C= MANE Select NP_000517.3:p.Gly48=
Search 100 bp 5'
Search 100 bp 3'