Canonical Allele Identifier: CA2260087070
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586843G= , CM000679.2:g.41586843G= GRCh38
NC_000017.10:g.39743095G= , CM000679.1:g.39743095G= GRCh37
NC_000017.9:g.36996621G= NCBI36
NG_008624.1:g.5053C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.-9C= MANE Select ENSP00000167586.6:n.-9C=
ENST00000167586.6:c.-9C= ENSP00000167586.6:n.-9C=
NM_000526.4:c.-9C= NP_000517.2:n.-9C=
NM_000526.5:c.-9C= MANE Select NP_000517.3:n.-9C=