Canonical Allele Identifier: CA399475363
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583274A>G , CM000679.2:g.41583274A>G GRCh38
NC_000017.10:g.39739526A>G , CM000679.1:g.39739526A>G GRCh37
NC_000017.9:g.36993052A>G NCBI36
NG_008624.1:g.8622T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1235T>C MANE Select ENSP00000167586.6:p.Ile412Thr
ENST00000167586.6:c.1235T>C ENSP00000167586.6:p.Ile412Thr
ENST00000441550.2:n.182T>C
ENST00000476662.1:n.685T>C
NM_000526.4:c.1235T>C NP_000517.2:p.Ile412Thr
NM_000526.5:c.1235T>C MANE Select NP_000517.3:p.Ile412Thr