Canonical Allele Identifier: CA2614443917
Gene: PACS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66211130del , CM000673.2:g.66211130del GRCh38
NC_000011.9:g.65978601del , CM000673.1:g.65978601del GRCh37
NC_000011.8:g.65735177del NCBI36
NG_033900.1:g.145778del

Transcript Alleles

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