Canonical Allele Identifier: CA2574883591
Gene: PACS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66211110T>C , CM000673.2:g.66211110T>C GRCh38
NC_000011.9:g.65978581T>C , CM000673.1:g.65978581T>C GRCh37
NC_000011.8:g.65735157T>C NCBI36
NG_033900.1:g.145758T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320580.9:c.535-24T>C MANE Select ENSP00000316454.4:n.535-24T>C
ENST00000320580.8:c.535-24T>C ENSP00000316454.4:n.535-24T>C
ENST00000527224.1:n.659-24T>C
ENST00000527380.1:c.241-24T>C ENSP00000432639.1:n.241-24T>C
ENST00000533756.5:c.226-24T>C ENSP00000437150.1:n.226-24T>C
NM_018026.3:c.535-24T>C NP_060496.2:n.535-24T>C
XM_011545162.1:c.214-24T>C XP_011543464.1:n.214-24T>C
XM_011545163.1:c.205-24T>C XP_011543465.1:n.205-24T>C
XM_011545164.1:c.196-24T>C XP_011543466.1:n.196-24T>C
XM_011545164.2:c.196-24T>C XP_011543466.1:n.196-24T>C
XR_001747924.1:n.746-24T>C
NM_018026.4:c.535-24T>C MANE Select NP_060496.2:n.535-24T>C