Canonical Allele Identifier: CA399475359
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583273G>C , CM000679.2:g.41583273G>C GRCh38
NC_000017.10:g.39739525G>C , CM000679.1:g.39739525G>C GRCh37
NC_000017.9:g.36993051G>C NCBI36
NG_008624.1:g.8623C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1236C>G MANE Select ENSP00000167586.6:p.Ile412Met
ENST00000167586.6:c.1236C>G ENSP00000167586.6:p.Ile412Met
ENST00000441550.2:n.183C>G
ENST00000476662.1:n.686C>G
NM_000526.4:c.1236C>G NP_000517.2:p.Ile412Met
NM_000526.5:c.1236C>G MANE Select NP_000517.3:p.Ile412Met