Canonical Allele Identifier: CA223456686
Gene: PACS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66193528A>G , CM000673.2:g.66193528A>G GRCh38
NC_000011.9:g.65960999A>G , CM000673.1:g.65960999A>G GRCh37
NC_000011.8:g.65717575A>G NCBI36
NG_033900.1:g.128176A>G

Transcript Alleles

HGVS Amino-acid Change
NM_018026.4:c.399A>G MANE Select NP_060496.2:p.Glu133=
ENST00000320580.9:c.399A>G MANE Select ENSP00000316454.4:p.Glu133=
NM_018026.3:c.399A>G NP_060496.2:p.Glu133=
ENST00000320580.8:c.399A>G ENSP00000316454.4:p.Glu133=
ENST00000527224.1:n.523A>G
ENST00000527380.1:c.105A>G ENSP00000432639.1:p.Glu35=
ENST00000533756.5:c.90A>G ENSP00000437150.1:p.Glu30=
XM_011545162.1:c.78A>G XP_011543464.1:p.Glu26=
XM_011545163.1:c.69A>G XP_011543465.1:p.Glu23=
XM_011545164.1:c.60A>G XP_011543466.1:p.Glu20=
XM_011545164.2:c.60A>G XP_011543466.1:p.Glu20=
XR_001747924.1:n.610A>G