Canonical Allele Identifier: CA2260086949
Gene: KRT14 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586654C= , CM000679.2:g.41586654C= GRCh38
NC_000017.10:g.39742906C= , CM000679.1:g.39742906C= GRCh37
NC_000017.9:g.36996432C= NCBI36
NG_008624.1:g.5242G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.181G= MANE Select ENSP00000167586.6:p.Gly61=
ENST00000167586.6:c.181G= ENSP00000167586.6:p.Gly61=
NM_000526.4:c.181G= NP_000517.2:p.Gly61=
NM_000526.5:c.181G= MANE Select NP_000517.3:p.Gly61=
Search 100 bp 5'
Search 100 bp 3'