Canonical Allele Identifier: CA224025891
Gene: PACS1 HGNC NCBI

Linked Data

dbSNP Id: rs112192900

Genomic Alleles

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

Transcript Alleles

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