Canonical Allele Identifier: CA1979579273

Gene: PACS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66211129C= , CM000673.2:g.66211129C=	GRCh38
NC_000011.9:g.65978600C= , CM000673.1:g.65978600C=	GRCh37
NC_000011.8:g.65735176C=	NCBI36
NG_033900.1:g.145777C=

Transcript Alleles

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