Canonical Allele Identifier: CA8562655
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs369639773

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584391G>T , CM000679.2:g.41584391G>T GRCh38
NC_000017.10:g.39740643G>T , CM000679.1:g.39740643G>T GRCh37
NC_000017.9:g.36994169G>T NCBI36
NG_008624.1:g.7505C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.631C>A MANE Select ENSP00000167586.6:p.Arg211Ser
ENST00000167586.6:c.631C>A ENSP00000167586.6:p.Arg211Ser
ENST00000476662.1:n.81C>A
NM_000526.4:c.631C>A NP_000517.2:p.Arg211Ser
NM_000526.5:c.631C>A MANE Select NP_000517.3:p.Arg211Ser