Canonical Allele Identifier: CA399476952
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1907419995

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583675G>A , CM000679.2:g.41583675G>A GRCh38
NC_000017.10:g.39739927G>A , CM000679.1:g.39739927G>A GRCh37
NC_000017.9:g.36993453G>A NCBI36
NG_008624.1:g.8221C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.929C>T MANE Select ENSP00000167586.6:p.Thr310Ile
ENST00000167586.6:c.929C>T ENSP00000167586.6:p.Thr310Ile
ENST00000476662.1:n.379C>T
NM_000526.4:c.929C>T NP_000517.2:p.Thr310Ile
NM_000526.5:c.929C>T MANE Select NP_000517.3:p.Thr310Ile