Canonical Allele Identifier: CA2260085269
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583198A= , CM000679.2:g.41583198A= GRCh38
NC_000017.10:g.39739450A= , CM000679.1:g.39739450A= GRCh37
NC_000017.9:g.36992976A= NCBI36
NG_008624.1:g.8698T=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1274+37T= MANE Select ENSP00000167586.6:n.1274+37T=
ENST00000167586.6:c.1274+37T= ENSP00000167586.6:n.1274+37T=
ENST00000441550.2:n.221+37T=
NM_000526.4:c.1274+37T= NP_000517.2:n.1274+37T=
NM_000526.5:c.1274+37T= MANE Select NP_000517.3:n.1274+37T=