Canonical Allele Identifier: CA2260085565
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583776T= , CM000679.2:g.41583776T= GRCh38
NC_000017.10:g.39740028T= , CM000679.1:g.39740028T= GRCh37
NC_000017.9:g.36993554T= NCBI36
NG_008624.1:g.8120A=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.911A= MANE Select ENSP00000167586.6:p.Glu304=
ENST00000167586.6:c.911A= ENSP00000167586.6:p.Glu304=
ENST00000476662.1:n.361A=
NM_000526.4:c.911A= NP_000517.2:p.Glu304=
NM_000526.5:c.911A= MANE Select NP_000517.3:p.Glu304=