Canonical Allele Identifier: CA399476969
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583677C>A , CM000679.2:g.41583677C>A GRCh38
NC_000017.10:g.39739929C>A , CM000679.1:g.39739929C>A GRCh37
NC_000017.9:g.36993455C>A NCBI36
NG_008624.1:g.8219G>T

Transcript Alleles

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