Canonical Allele Identifier: CA399478135
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584321T>G , CM000679.2:g.41584321T>G GRCh38
NC_000017.10:g.39740573T>G , CM000679.1:g.39740573T>G GRCh37
NC_000017.9:g.36994099T>G NCBI36
NG_008624.1:g.7575A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.701A>C MANE Select ENSP00000167586.6:p.Asp234Ala
ENST00000167586.6:c.701A>C ENSP00000167586.6:p.Asp234Ala
ENST00000476662.1:n.151A>C
NM_000526.4:c.701A>C NP_000517.2:p.Asp234Ala
NM_000526.5:c.701A>C MANE Select NP_000517.3:p.Asp234Ala