Canonical Allele Identifier: CA1979579254

Gene: PACS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66211112G= , CM000673.2:g.66211112G=	GRCh38
NC_000011.9:g.65978583G= , CM000673.1:g.65978583G=	GRCh37
NC_000011.8:g.65735159G=	NCBI36
NG_033900.1:g.145760G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.535-22G= MANE Select	ENSP00000316454.4:n.535-22G=
ENST00000320580.8:c.535-22G=	ENSP00000316454.4:n.535-22G=
ENST00000527224.1:n.659-22G=
ENST00000527380.1:c.241-22G=	ENSP00000432639.1:n.241-22G=
ENST00000533756.5:c.226-22G=	ENSP00000437150.1:n.226-22G=
NM_018026.3:c.535-22G=	NP_060496.2:n.535-22G=
XM_011545162.1:c.214-22G=	XP_011543464.1:n.214-22G=
XM_011545163.1:c.205-22G=	XP_011543465.1:n.205-22G=
XM_011545164.1:c.196-22G=	XP_011543466.1:n.196-22G=
XM_011545164.2:c.196-22G=	XP_011543466.1:n.196-22G=
XR_001747924.1:n.746-22G=
NM_018026.4:c.535-22G= MANE Select	NP_060496.2:n.535-22G=