Canonical Allele Identifier: CA2260085447
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583538G= , CM000679.2:g.41583538G= GRCh38
NC_000017.10:g.39739790G= , CM000679.1:g.39739790G= GRCh37
NC_000017.9:g.36993316G= NCBI36
NG_008624.1:g.8358C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1053+13C= MANE Select ENSP00000167586.6:n.1053+13C=
ENST00000167586.6:c.1053+13C= ENSP00000167586.6:n.1053+13C=
ENST00000476662.1:n.503+13C=
NM_000526.4:c.1053+13C= NP_000517.2:n.1053+13C=
NM_000526.5:c.1053+13C= MANE Select NP_000517.3:n.1053+13C=