Canonical Allele Identifier: CA6116324
Gene: PACS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66216169C>T , CM000673.2:g.66216169C>T GRCh38
NC_000011.9:g.65983640C>T , CM000673.1:g.65983640C>T GRCh37
NC_000011.8:g.65740216C>T NCBI36
NG_033900.1:g.150817C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320580.9:c.711C>T MANE Select ENSP00000316454.4:p.Asn237=
ENST00000320580.8:c.711C>T ENSP00000316454.4:p.Asn237=
ENST00000527224.1:n.835C>T
ENST00000527380.1:c.417C>T ENSP00000432639.1:p.Asn139=
NM_018026.3:c.711C>T NP_060496.2:p.Asn237=
XM_011545162.1:c.390C>T XP_011543464.1:p.Asn130=
XM_011545163.1:c.381C>T XP_011543465.1:p.Asn127=
XM_011545164.1:c.372C>T XP_011543466.1:p.Asn124=
XM_011545164.2:c.372C>T XP_011543466.1:p.Asn124=
XR_001747924.1:n.922C>T
NM_018026.4:c.711C>T MANE Select NP_060496.2:p.Asn237=