Canonical Allele Identifier: CA399476642
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583618C>G , CM000679.2:g.41583618C>G GRCh38
NC_000017.10:g.39739870C>G , CM000679.1:g.39739870C>G GRCh37
NC_000017.9:g.36993396C>G NCBI36
NG_008624.1:g.8278G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.986G>C MANE Select ENSP00000167586.6:p.Ser329Thr
ENST00000167586.6:c.986G>C ENSP00000167586.6:p.Ser329Thr
ENST00000476662.1:n.436G>C
NM_000526.4:c.986G>C NP_000517.2:p.Ser329Thr
NM_000526.5:c.986G>C MANE Select NP_000517.3:p.Ser329Thr