Canonical Allele Identifier: CA1979644176
Gene: PACS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66241918T= , CM000673.2:g.66241918T= GRCh38
NC_000011.9:g.66009389T= , CM000673.1:g.66009389T= GRCh37
NC_000011.8:g.65765965T= NCBI36
NG_033900.1:g.176566T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320580.9:c.2656+265T= MANE Select ENSP00000316454.4:n.2656+265T=
ENST00000320580.8:c.2656+265T= ENSP00000316454.4:n.2656+265T=
ENST00000524815.5:c.40+265T= ENSP00000433991.1:n.40+265T=
ENST00000529677.1:c.206+265T=
ENST00000529757.5:c.1264+265T= ENSP00000432858.1:n.1264+265T=
ENST00000531597.1:c.40+265T= ENSP00000434012.1:n.40+265T=
NM_018026.3:c.2656+265T= NP_060496.2:n.2656+265T=
XM_011545162.1:c.2335+265T= XP_011543464.1:n.2335+265T=
XM_011545163.1:c.2326+265T= XP_011543465.1:n.2326+265T=
XM_011545164.1:c.2317+265T= XP_011543466.1:n.2317+265T=
XM_011545164.2:c.2317+265T= XP_011543466.1:n.2317+265T=
NM_018026.4:c.2656+265T= MANE Select NP_060496.2:n.2656+265T=