Canonical Allele Identifier: CA399483252
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586678A>C , CM000679.2:g.41586678A>C GRCh38
NC_000017.10:g.39742930A>C , CM000679.1:g.39742930A>C GRCh37
NC_000017.9:g.36996456A>C NCBI36
NG_008624.1:g.5218T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.157T>G MANE Select ENSP00000167586.6:p.Ser53Ala
ENST00000167586.6:c.157T>G ENSP00000167586.6:p.Ser53Ala
NM_000526.4:c.157T>G NP_000517.2:p.Ser53Ala
NM_000526.5:c.157T>G MANE Select NP_000517.3:p.Ser53Ala