Canonical Allele Identifier: CA475299536
Gene: PACS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66210406T>A , CM000673.2:g.66210406T>A GRCh38
NC_000011.9:g.65977877T>A , CM000673.1:g.65977877T>A GRCh37
NC_000011.8:g.65734453T>A NCBI36
NG_033900.1:g.145054T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320580.9:c.489T>A MANE Select ENSP00000316454.4:p.Ala163=
ENST00000320580.8:c.489T>A ENSP00000316454.4:p.Ala163=
ENST00000527224.1:n.613T>A
ENST00000527380.1:c.195T>A ENSP00000432639.1:p.Ala65=
ENST00000533756.5:c.180T>A ENSP00000437150.1:p.Ala60=
NM_018026.3:c.489T>A NP_060496.2:p.Ala163=
XM_011545162.1:c.168T>A XP_011543464.1:p.Ala56=
XM_011545163.1:c.159T>A XP_011543465.1:p.Ala53=
XM_011545164.1:c.150T>A XP_011543466.1:p.Ala50=
XM_011545164.2:c.150T>A XP_011543466.1:p.Ala50=
XR_001747924.1:n.700T>A
NM_018026.4:c.489T>A MANE Select NP_060496.2:p.Ala163=