Canonical Allele Identifier: CA384973369
Gene: KRT75 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433811T>G , CM000674.2:g.52433811T>G GRCh38
NC_000012.11:g.52827595T>G , CM000674.1:g.52827595T>G GRCh37
NC_000012.10:g.51113862T>G NCBI36
NG_008403.1:g.5516A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.494A>C MANE Select ENSP00000252245.5:p.Asp165Ala
ENST00000252245.5:c.494A>C ENSP00000252245.5:p.Asp165Ala
NM_004693.2:c.494A>C NP_004684.2:p.Asp165Ala
NM_004693.3:c.494A>C MANE Select NP_004684.2:p.Asp165Ala