Canonical Allele Identifier: CA399477152
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583786C>G , CM000679.2:g.41583786C>G GRCh38
NC_000017.10:g.39740038C>G , CM000679.1:g.39740038C>G GRCh37
NC_000017.9:g.36993564C>G NCBI36
NG_008624.1:g.8110G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.901G>C MANE Select ENSP00000167586.6:p.Asp301His
ENST00000167586.6:c.901G>C ENSP00000167586.6:p.Asp301His
ENST00000476662.1:n.351G>C
NM_000526.4:c.901G>C NP_000517.2:p.Asp301His
NM_000526.5:c.901G>C MANE Select NP_000517.3:p.Asp301His