Canonical Allele Identifier: CA1979579269

Gene: PACS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66211124T= , CM000673.2:g.66211124T=	GRCh38
NC_000011.9:g.65978595T= , CM000673.1:g.65978595T=	GRCh37
NC_000011.8:g.65735171T=	NCBI36
NG_033900.1:g.145772T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.535-10T= MANE Select	ENSP00000316454.4:n.535-10T=
ENST00000320580.8:c.535-10T=	ENSP00000316454.4:n.535-10T=
ENST00000527224.1:n.659-10T=
ENST00000527380.1:c.241-10T=	ENSP00000432639.1:n.241-10T=
ENST00000533756.5:c.226-10T=	ENSP00000437150.1:n.226-10T=
NM_018026.3:c.535-10T=	NP_060496.2:n.535-10T=
XM_011545162.1:c.214-10T=	XP_011543464.1:n.214-10T=
XM_011545163.1:c.205-10T=	XP_011543465.1:n.205-10T=
XM_011545164.1:c.196-10T=	XP_011543466.1:n.196-10T=
XM_011545164.2:c.196-10T=	XP_011543466.1:n.196-10T=
XR_001747924.1:n.746-10T=
NM_018026.4:c.535-10T= MANE Select	NP_060496.2:n.535-10T=