Canonical Allele Identifier: CA290665657
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs550076306

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586692C>T , CM000679.2:g.41586692C>T GRCh38
NC_000017.10:g.39742944C>T , CM000679.1:g.39742944C>T GRCh37
NC_000017.9:g.36996470C>T NCBI36
NG_008624.1:g.5204G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.143G>A MANE Select ENSP00000167586.6:p.Gly48Asp
ENST00000167586.6:c.143G>A ENSP00000167586.6:p.Gly48Asp
NM_000526.4:c.143G>A NP_000517.2:p.Gly48Asp
NM_000526.5:c.143G>A MANE Select NP_000517.3:p.Gly48Asp