Canonical Allele Identifier: CA1979579380
Gene: PACS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66211208G= , CM000673.2:g.66211208G= GRCh38
NC_000011.9:g.65978679G= , CM000673.1:g.65978679G= GRCh37
NC_000011.8:g.65735255G= NCBI36
NG_033900.1:g.145856G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320580.9:c.609G= MANE Select ENSP00000316454.4:p.Arg203=
ENST00000320580.8:c.609G= ENSP00000316454.4:p.Arg203=
ENST00000527224.1:n.733G=
ENST00000527380.1:c.315G= ENSP00000432639.1:p.Arg105=
ENST00000533756.5:c.300G= ENSP00000437150.1:p.Arg100=
NM_018026.3:c.609G= NP_060496.2:p.Arg203=
XM_011545162.1:c.288G= XP_011543464.1:p.Arg96=
XM_011545163.1:c.279G= XP_011543465.1:p.Arg93=
XM_011545164.1:c.270G= XP_011543466.1:p.Arg90=
XM_011545164.2:c.270G= XP_011543466.1:p.Arg90=
XR_001747924.1:n.820G=
NM_018026.4:c.609G= MANE Select NP_060496.2:p.Arg203=