Canonical Allele Identifier: CA6116389

Gene: PACS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66216754C>G , CM000673.2:g.66216754C>G	GRCh38
NC_000011.9:g.65984225C>G , CM000673.1:g.65984225C>G	GRCh37
NC_000011.8:g.65740801C>G	NCBI36
NG_033900.1:g.151402C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.957C>G MANE Select	ENSP00000316454.4:p.Thr319=
ENST00000320580.8:c.957C>G	ENSP00000316454.4:p.Thr319=
ENST00000524784.1:c.129C>G	ENSP00000435037.1:p.Thr43=
ENST00000527224.1:n.1081C>G
ENST00000531298.5:c.218C>G
NM_018026.3:c.957C>G	NP_060496.2:p.Thr319=
XM_011545162.1:c.636C>G	XP_011543464.1:p.Thr212=
XM_011545163.1:c.627C>G	XP_011543465.1:p.Thr209=
XM_011545164.1:c.618C>G	XP_011543466.1:p.Thr206=
XM_011545164.2:c.618C>G	XP_011543466.1:p.Thr206=
XR_001747924.1:n.1168C>G
NM_018026.4:c.957C>G MANE Select	NP_060496.2:p.Thr319=