Canonical Allele Identifier: CA399477391
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583826C>G , CM000679.2:g.41583826C>G GRCh38
NC_000017.10:g.39740078C>G , CM000679.1:g.39740078C>G GRCh37
NC_000017.9:g.36993604C>G NCBI36
NG_008624.1:g.8070G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.861G>C MANE Select ENSP00000167586.6:p.Met287Ile
ENST00000167586.6:c.861G>C ENSP00000167586.6:p.Met287Ile
ENST00000476662.1:n.311G>C
NM_000526.4:c.861G>C NP_000517.2:p.Met287Ile
NM_000526.5:c.861G>C MANE Select NP_000517.3:p.Met287Ile