Canonical Allele Identifier: CA399483490
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586722C>G , CM000679.2:g.41586722C>G GRCh38
NC_000017.10:g.39742974C>G , CM000679.1:g.39742974C>G GRCh37
NC_000017.9:g.36996500C>G NCBI36
NG_008624.1:g.5174G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.113G>C MANE Select ENSP00000167586.6:p.Gly38Ala
ENST00000167586.6:c.113G>C ENSP00000167586.6:p.Gly38Ala
NM_000526.4:c.113G>C NP_000517.2:p.Gly38Ala
NM_000526.5:c.113G>C MANE Select NP_000517.3:p.Gly38Ala