Canonical Allele Identifier: CA2637834065
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583028G>A , CM000679.2:g.41583028G>A GRCh38
NC_000017.10:g.39739280G>A , CM000679.1:g.39739280G>A GRCh37
NC_000017.9:g.36992806G>A NCBI36
NG_008624.1:g.8868C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1321+66C>T MANE Select ENSP00000167586.6:n.1321+66C>T
ENST00000167586.6:c.1321+66C>T ENSP00000167586.6:n.1321+66C>T
ENST00000441550.2:n.334C>T
NM_000526.4:c.1321+66C>T NP_000517.2:n.1321+66C>T
NM_000526.5:c.1321+66C>T MANE Select NP_000517.3:n.1321+66C>T