Canonical Allele Identifier: CA2260087071
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586844G= , CM000679.2:g.41586844G= GRCh38
NC_000017.10:g.39743096G= , CM000679.1:g.39743096G= GRCh37
NC_000017.9:g.36996622G= NCBI36
NG_008624.1:g.5052C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.-10C= MANE Select ENSP00000167586.6:n.-10C=
ENST00000167586.6:c.-10C= ENSP00000167586.6:n.-10C=
NM_000526.4:c.-10C= NP_000517.2:n.-10C=
NM_000526.5:c.-10C= MANE Select NP_000517.3:n.-10C=