Canonical Allele Identifier: CA6580151
Gene: KRT75 HGNC NCBI

Linked Data

dbSNP Id: rs750520382

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433866C>A , CM000674.2:g.52433866C>A GRCh38
NC_000012.11:g.52827650C>A , CM000674.1:g.52827650C>A GRCh37
NC_000012.10:g.51113917C>A NCBI36
NG_008403.1:g.5461G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.439G>T MANE Select ENSP00000252245.5:p.Ala147Ser
ENST00000252245.5:c.439G>T ENSP00000252245.5:p.Ala147Ser
NM_004693.2:c.439G>T NP_004684.2:p.Ala147Ser
NM_004693.3:c.439G>T MANE Select NP_004684.2:p.Ala147Ser