Canonical Allele Identifier: CA399475709
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1467006522

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583341C>T , CM000679.2:g.41583341C>T GRCh38
NC_000017.10:g.39739593C>T , CM000679.1:g.39739593C>T GRCh37
NC_000017.9:g.36993119C>T NCBI36
NG_008624.1:g.8555G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1168G>A MANE Select ENSP00000167586.6:p.Glu390Lys
ENST00000167586.6:c.1168G>A ENSP00000167586.6:p.Glu390Lys
ENST00000441550.2:n.115G>A
ENST00000476662.1:n.618G>A
NM_000526.4:c.1168G>A NP_000517.2:p.Glu390Lys
NM_000526.5:c.1168G>A MANE Select NP_000517.3:p.Glu390Lys