Canonical Allele Identifier: CA1979644135
Gene: PACS1 HGNC NCBI

Linked Data

dbSNP Id: rs1855820693

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66241811G>A , CM000673.2:g.66241811G>A GRCh38
NC_000011.9:g.66009282G>A , CM000673.1:g.66009282G>A GRCh37
NC_000011.8:g.65765858G>A NCBI36
NG_033900.1:g.176459G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320580.9:c.2656+158G>A MANE Select ENSP00000316454.4:n.2656+158G>A
ENST00000320580.8:c.2656+158G>A ENSP00000316454.4:n.2656+158G>A
ENST00000524815.5:c.40+158G>A ENSP00000433991.1:n.40+158G>A
ENST00000529677.1:c.206+158G>A
ENST00000529757.5:c.1264+158G>A ENSP00000432858.1:n.1264+158G>A
ENST00000531597.1:c.40+158G>A ENSP00000434012.1:n.40+158G>A
NM_018026.3:c.2656+158G>A NP_060496.2:n.2656+158G>A
XM_011545162.1:c.2335+158G>A XP_011543464.1:n.2335+158G>A
XM_011545163.1:c.2326+158G>A XP_011543465.1:n.2326+158G>A
XM_011545164.1:c.2317+158G>A XP_011543466.1:n.2317+158G>A
XM_011545164.2:c.2317+158G>A XP_011543466.1:n.2317+158G>A
NM_018026.4:c.2656+158G>A MANE Select NP_060496.2:n.2656+158G>A