Canonical Allele Identifier: CA1979644132
Gene: PACS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66241808C= , CM000673.2:g.66241808C= GRCh38
NC_000011.9:g.66009279C= , CM000673.1:g.66009279C= GRCh37
NC_000011.8:g.65765855C= NCBI36
NG_033900.1:g.176456C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320580.9:c.2656+155C= MANE Select ENSP00000316454.4:n.2656+155C=
ENST00000320580.8:c.2656+155C= ENSP00000316454.4:n.2656+155C=
ENST00000524815.5:c.40+155C= ENSP00000433991.1:n.40+155C=
ENST00000529677.1:c.206+155C=
ENST00000529757.5:c.1264+155C= ENSP00000432858.1:n.1264+155C=
ENST00000531597.1:c.40+155C= ENSP00000434012.1:n.40+155C=
NM_018026.3:c.2656+155C= NP_060496.2:n.2656+155C=
XM_011545162.1:c.2335+155C= XP_011543464.1:n.2335+155C=
XM_011545163.1:c.2326+155C= XP_011543465.1:n.2326+155C=
XM_011545164.1:c.2317+155C= XP_011543466.1:n.2317+155C=
XM_011545164.2:c.2317+155C= XP_011543466.1:n.2317+155C=
NM_018026.4:c.2656+155C= MANE Select NP_060496.2:n.2656+155C=