Canonical Allele Identifier: CA2618923496
Gene: KRT75 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433786del , CM000674.2:g.52433786del GRCh38
NC_000012.11:g.52827570del , CM000674.1:g.52827570del GRCh37
NC_000012.10:g.51113837del NCBI36
NG_008403.1:g.5545del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.498+25del MANE Select ENSP00000252245.5:n.498+25del
ENST00000252245.5:c.498+25del ENSP00000252245.5:n.498+25del
NM_004693.2:c.498+25del NP_004684.2:n.498+25del
NM_004693.3:c.498+25del MANE Select NP_004684.2:n.498+25del