Canonical Allele Identifier: CA399476607
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583612A>G , CM000679.2:g.41583612A>G GRCh38
NC_000017.10:g.39739864A>G , CM000679.1:g.39739864A>G GRCh37
NC_000017.9:g.36993390A>G NCBI36
NG_008624.1:g.8284T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.992T>C MANE Select ENSP00000167586.6:p.Ile331Thr
ENST00000167586.6:c.992T>C ENSP00000167586.6:p.Ile331Thr
ENST00000476662.1:n.442T>C
NM_000526.4:c.992T>C NP_000517.2:p.Ile331Thr
NM_000526.5:c.992T>C MANE Select NP_000517.3:p.Ile331Thr