Canonical Allele Identifier: CA399477191
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583793G>C , CM000679.2:g.41583793G>C GRCh38
NC_000017.10:g.39740045G>C , CM000679.1:g.39740045G>C GRCh37
NC_000017.9:g.36993571G>C NCBI36
NG_008624.1:g.8103C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.894C>G MANE Select ENSP00000167586.6:p.Asn298Lys
ENST00000167586.6:c.894C>G ENSP00000167586.6:p.Asn298Lys
ENST00000476662.1:n.344C>G
NM_000526.4:c.894C>G NP_000517.2:p.Asn298Lys
NM_000526.5:c.894C>G MANE Select NP_000517.3:p.Asn298Lys