Canonical Allele Identifier: CA2260085281
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583207G= , CM000679.2:g.41583207G= GRCh38
NC_000017.10:g.39739459G= , CM000679.1:g.39739459G= GRCh37
NC_000017.9:g.36992985G= NCBI36
NG_008624.1:g.8689C=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1274+28C= MANE Select ENSP00000167586.6:n.1274+28C=
ENST00000167586.6:c.1274+28C= ENSP00000167586.6:n.1274+28C=
ENST00000441550.2:n.221+28C=
NM_000526.4:c.1274+28C= NP_000517.2:n.1274+28C=
NM_000526.5:c.1274+28C= MANE Select NP_000517.3:n.1274+28C=