Canonical Allele Identifier: CA2036511550
Gene: KRT75 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433857G= , CM000674.2:g.52433857G= GRCh38
NC_000012.11:g.52827641G= , CM000674.1:g.52827641G= GRCh37
NC_000012.10:g.51113908G= NCBI36
NG_008403.1:g.5470C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.448C= MANE Select ENSP00000252245.5:p.Arg150=
ENST00000252245.5:c.448C= ENSP00000252245.5:p.Arg150=
NM_004693.2:c.448C= NP_004684.2:p.Arg150=
NM_004693.3:c.448C= MANE Select NP_004684.2:p.Arg150=