Canonical Allele Identifier: CA2260086842
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586480T= , CM000679.2:g.41586480T= GRCh38
NC_000017.10:g.39742732T= , CM000679.1:g.39742732T= GRCh37
NC_000017.9:g.36996258T= NCBI36
NG_008624.1:g.5416A=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.355A= MANE Select ENSP00000167586.6:p.Met119=
ENST00000167586.6:c.355A= ENSP00000167586.6:p.Met119=
NM_000526.4:c.355A= NP_000517.2:p.Met119=
NM_000526.5:c.355A= MANE Select NP_000517.3:p.Met119=