Canonical Allele Identifier: CA2260086981
Gene: KRT14 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586705T= , CM000679.2:g.41586705T= GRCh38
NC_000017.10:g.39742957T= , CM000679.1:g.39742957T= GRCh37
NC_000017.9:g.36996483T= NCBI36
NG_008624.1:g.5191A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.130A= MANE Select ENSP00000167586.6:p.Ser44=
ENST00000167586.6:c.130A= ENSP00000167586.6:p.Ser44=
NM_000526.4:c.130A= NP_000517.2:p.Ser44=
NM_000526.5:c.130A= MANE Select NP_000517.3:p.Ser44=
Search 100 bp 5'
Search 100 bp 3'