Canonical Allele Identifier: CA399476468
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1907413156

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583585T>G , CM000679.2:g.41583585T>G GRCh38
NC_000017.10:g.39739837T>G , CM000679.1:g.39739837T>G GRCh37
NC_000017.9:g.36993363T>G NCBI36
NG_008624.1:g.8311A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1019A>C MANE Select ENSP00000167586.6:p.Asn340Thr
ENST00000167586.6:c.1019A>C ENSP00000167586.6:p.Asn340Thr
ENST00000476662.1:n.469A>C
NM_000526.4:c.1019A>C NP_000517.2:p.Asn340Thr
NM_000526.5:c.1019A>C MANE Select NP_000517.3:p.Asn340Thr