Canonical Allele Identifier: CA2839451775
Gene: KRT75 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433746dup , CM000674.2:g.52433746dup GRCh38
NC_000012.11:g.52827530dup , CM000674.1:g.52827530dup GRCh37
NC_000012.10:g.51113797dup NCBI36
NG_008403.1:g.5581dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.498+61dup MANE Select ENSP00000252245.5:n.498+61dup
ENST00000252245.5:c.498+61dup ENSP00000252245.5:n.498+61dup
NM_004693.2:c.498+61dup NP_004684.2:n.498+61dup
NM_004693.3:c.498+61dup MANE Select NP_004684.2:n.498+61dup