Canonical Allele Identifier: CA2036511593
Gene: KRT75 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433874C= , CM000674.2:g.52433874C= GRCh38
NC_000012.11:g.52827658C= , CM000674.1:g.52827658C= GRCh37
NC_000012.10:g.51113925C= NCBI36
NG_008403.1:g.5453G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.431G= MANE Select ENSP00000252245.5:p.Arg144=
ENST00000252245.5:c.431G= ENSP00000252245.5:p.Arg144=
NM_004693.2:c.431G= NP_004684.2:p.Arg144=
NM_004693.3:c.431G= MANE Select NP_004684.2:p.Arg144=