Canonical Allele Identifier: CA8562844
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs765738033

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586831T>C , CM000679.2:g.41586831T>C GRCh38
NC_000017.10:g.39743083T>C , CM000679.1:g.39743083T>C GRCh37
NC_000017.9:g.36996609T>C NCBI36
NG_008624.1:g.5065A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.4A>G MANE Select ENSP00000167586.6:p.Thr2Ala
ENST00000167586.6:c.4A>G ENSP00000167586.6:p.Thr2Ala
NM_000526.4:c.4A>G NP_000517.2:p.Thr2Ala
NM_000526.5:c.4A>G MANE Select NP_000517.3:p.Thr2Ala