Canonical Allele Identifier: CA399476775
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1907417778

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583644G>C , CM000679.2:g.41583644G>C GRCh38
NC_000017.10:g.39739896G>C , CM000679.1:g.39739896G>C GRCh37
NC_000017.9:g.36993422G>C NCBI36
NG_008624.1:g.8252C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.960C>G MANE Select ENSP00000167586.6:p.Asn320Lys
ENST00000167586.6:c.960C>G ENSP00000167586.6:p.Asn320Lys
ENST00000476662.1:n.410C>G
NM_000526.4:c.960C>G NP_000517.2:p.Asn320Lys
NM_000526.5:c.960C>G MANE Select NP_000517.3:p.Asn320Lys