Canonical Allele Identifier: CA290664962
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs113144130

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583679G>C , CM000679.2:g.41583679G>C GRCh38
NC_000017.10:g.39739931G>C , CM000679.1:g.39739931G>C GRCh37
NC_000017.9:g.36993457G>C NCBI36
NG_008624.1:g.8217C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.928-3C>G MANE Select ENSP00000167586.6:n.928-3C>G
ENST00000167586.6:c.928-3C>G ENSP00000167586.6:n.928-3C>G
ENST00000476662.1:n.378-3C>G
NM_000526.4:c.928-3C>G NP_000517.2:n.928-3C>G
NM_000526.5:c.928-3C>G MANE Select NP_000517.3:n.928-3C>G