Canonical Allele Identifier: CA2581308316
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583020T>C , CM000679.2:g.41583020T>C GRCh38
NC_000017.10:g.39739272T>C , CM000679.1:g.39739272T>C GRCh37
NC_000017.9:g.36992798T>C NCBI36
NG_008624.1:g.8876A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1321+74A>G MANE Select ENSP00000167586.6:n.1321+74A>G
ENST00000167586.6:c.1321+74A>G ENSP00000167586.6:n.1321+74A>G
ENST00000441550.2:n.342A>G
NM_000526.4:c.1321+74A>G NP_000517.2:n.1321+74A>G
NM_000526.5:c.1321+74A>G MANE Select NP_000517.3:n.1321+74A>G