Canonical Allele Identifier: CA6116313
Community Standard Title: NM_018026.4(PACS1):c.661-5C>G
Gene: PACS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66216114C>G , CM000673.2:g.66216114C>G GRCh38
NC_000011.9:g.65983585C>G , CM000673.1:g.65983585C>G GRCh37
NC_000011.8:g.65740161C>G NCBI36
NG_033900.1:g.150762C>G

Transcript Alleles

HGVS Amino-acid Change
NM_018026.4:c.661-5C>G MANE Select NP_060496.2:n.661-5C>G
ENST00000320580.9:c.661-5C>G MANE Select ENSP00000316454.4:n.661-5C>G
NM_018026.3:c.661-5C>G NP_060496.2:n.661-5C>G
ENST00000320580.8:c.661-5C>G ENSP00000316454.4:n.661-5C>G
ENST00000527224.1:n.785-5C>G
ENST00000527380.1:c.367-5C>G ENSP00000432639.1:n.367-5C>G
XM_011545162.1:c.340-5C>G XP_011543464.1:n.340-5C>G
XM_011545163.1:c.331-5C>G XP_011543465.1:n.331-5C>G
XM_011545164.1:c.322-5C>G XP_011543466.1:n.322-5C>G
XM_011545164.2:c.322-5C>G XP_011543466.1:n.322-5C>G
XR_001747924.1:n.872-5C>G