Canonical Allele Identifier: CA2036511374
Gene: KRT75 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433733T= , CM000674.2:g.52433733T= GRCh38
NC_000012.11:g.52827517T= , CM000674.1:g.52827517T= GRCh37
NC_000012.10:g.51113784T= NCBI36
NG_008403.1:g.5594A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.498+74A= MANE Select ENSP00000252245.5:n.498+74A=
ENST00000252245.5:c.498+74A= ENSP00000252245.5:n.498+74A=
NM_004693.2:c.498+74A= NP_004684.2:n.498+74A=
NM_004693.3:c.498+74A= MANE Select NP_004684.2:n.498+74A=