Canonical Allele Identifier: CA2260085546
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583736C= , CM000679.2:g.41583736C= GRCh38
NC_000017.10:g.39739988C= , CM000679.1:g.39739988C= GRCh37
NC_000017.9:g.36993514C= NCBI36
NG_008624.1:g.8160G=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.927+24G= MANE Select ENSP00000167586.6:n.927+24G=
ENST00000167586.6:c.927+24G= ENSP00000167586.6:n.927+24G=
ENST00000476662.1:n.377+24G=
NM_000526.4:c.927+24G= NP_000517.2:n.927+24G=
NM_000526.5:c.927+24G= MANE Select NP_000517.3:n.927+24G=