Canonical Allele Identifier: CA399482049
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586378T>C , CM000679.2:g.41586378T>C GRCh38
NC_000017.10:g.39742630T>C , CM000679.1:g.39742630T>C GRCh37
NC_000017.9:g.36996156T>C NCBI36
NG_008624.1:g.5518A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.457A>G MANE Select ENSP00000167586.6:p.Arg153Gly
ENST00000167586.6:c.457A>G ENSP00000167586.6:p.Arg153Gly
NM_000526.4:c.457A>G NP_000517.2:p.Arg153Gly
NM_000526.5:c.457A>G MANE Select NP_000517.3:p.Arg153Gly