Canonical Allele Identifier: CA1261057162
Gene: NAT8 HGNC NCBI
ALMS1P1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73641112C= , CM000664.2:g.73641112C= GRCh38
NC_000002.11:g.73868239C= , CM000664.1:g.73868239C= GRCh37
NC_000002.10:g.73721747C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000272425.4:c.517G= (NAT8) MANE Select ENSP00000272425.3:p.Val173=
ENST00000652439.1:n.30C= (ALMS1P1)
ENST00000272425.3:c.517G= (NAT8) ENSP00000272425.3:p.Val173=
NM_003960.3:c.517G= (NAT8) NP_003951.3:p.Val173=
NM_003960.4:c.517G= (NAT8) MANE Select NP_003951.3:p.Val173=