Canonical Allele Identifier: CA1979579256
Gene: PACS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66211115T= , CM000673.2:g.66211115T= GRCh38
NC_000011.9:g.65978586T= , CM000673.1:g.65978586T= GRCh37
NC_000011.8:g.65735162T= NCBI36
NG_033900.1:g.145763T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320580.9:c.535-19T= MANE Select ENSP00000316454.4:n.535-19T=
ENST00000320580.8:c.535-19T= ENSP00000316454.4:n.535-19T=
ENST00000527224.1:n.659-19T=
ENST00000527380.1:c.241-19T= ENSP00000432639.1:n.241-19T=
ENST00000533756.5:c.226-19T= ENSP00000437150.1:n.226-19T=
NM_018026.3:c.535-19T= NP_060496.2:n.535-19T=
XM_011545162.1:c.214-19T= XP_011543464.1:n.214-19T=
XM_011545163.1:c.205-19T= XP_011543465.1:n.205-19T=
XM_011545164.1:c.196-19T= XP_011543466.1:n.196-19T=
XM_011545164.2:c.196-19T= XP_011543466.1:n.196-19T=
XR_001747924.1:n.746-19T=
NM_018026.4:c.535-19T= MANE Select NP_060496.2:n.535-19T=