Canonical Allele Identifier: CA6116306
Community Standard Title: NM_018026.4(PACS1):c.661-27G>T
Gene: PACS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66216092G>T , CM000673.2:g.66216092G>T GRCh38
NC_000011.9:g.65983563G>T , CM000673.1:g.65983563G>T GRCh37
NC_000011.8:g.65740139G>T NCBI36
NG_033900.1:g.150740G>T

Transcript Alleles

HGVS Amino-acid Change
NM_018026.4:c.661-27G>T MANE Select NP_060496.2:n.661-27G>T
ENST00000320580.9:c.661-27G>T MANE Select ENSP00000316454.4:n.661-27G>T
NM_018026.3:c.661-27G>T NP_060496.2:n.661-27G>T
ENST00000320580.8:c.661-27G>T ENSP00000316454.4:n.661-27G>T
ENST00000527224.1:n.785-27G>T
ENST00000527380.1:c.367-27G>T ENSP00000432639.1:n.367-27G>T
XM_011545162.1:c.340-27G>T XP_011543464.1:n.340-27G>T
XM_011545163.1:c.331-27G>T XP_011543465.1:n.331-27G>T
XM_011545164.1:c.322-27G>T XP_011543466.1:n.322-27G>T
XM_011545164.2:c.322-27G>T XP_011543466.1:n.322-27G>T
XR_001747924.1:n.872-27G>T