Canonical Allele Identifier: CA8562427
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs374916825

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583185C>T , CM000679.2:g.41583185C>T GRCh38
NC_000017.10:g.39739437C>T , CM000679.1:g.39739437C>T GRCh37
NC_000017.9:g.36992963C>T NCBI36
NG_008624.1:g.8711G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1275-45G>A MANE Select ENSP00000167586.6:n.1275-45G>A
ENST00000167586.6:c.1275-45G>A ENSP00000167586.6:n.1275-45G>A
ENST00000441550.2:n.222-45G>A
NM_000526.4:c.1275-45G>A NP_000517.2:n.1275-45G>A
NM_000526.5:c.1275-45G>A MANE Select NP_000517.3:n.1275-45G>A