Canonical Allele Identifier: CA2260087083
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586866G= , CM000679.2:g.41586866G= GRCh38
NC_000017.10:g.39743118G= , CM000679.1:g.39743118G= GRCh37
NC_000017.9:g.36996644G= NCBI36
NG_008624.1:g.5030C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.-32C= MANE Select ENSP00000167586.6:n.-32C=
ENST00000167586.6:c.-32C= ENSP00000167586.6:n.-32C=
NM_000526.4:c.-32C= NP_000517.2:n.-32C=
NM_000526.5:c.-32C= MANE Select NP_000517.3:n.-32C=