Canonical Allele Identifier: CA1979644060

Gene: PACS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66241617G= , CM000673.2:g.66241617G=	GRCh38
NC_000011.9:g.66009088G= , CM000673.1:g.66009088G=	GRCh37
NC_000011.8:g.65765664G=	NCBI36
NG_033900.1:g.176265G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.2620G= MANE Select	ENSP00000316454.4:p.Ala874=
ENST00000320580.8:c.2620G=	ENSP00000316454.4:p.Ala874=
ENST00000524815.5:c.4G=	ENSP00000433991.1:p.Ala2=
ENST00000529677.1:c.170G=
ENST00000529757.5:c.1228G=	ENSP00000432858.1:p.Ala410=
ENST00000531597.1:c.4G=	ENSP00000434012.1:p.Ala2=
NM_018026.3:c.2620G=	NP_060496.2:p.Ala874=
XM_011545162.1:c.2299G=	XP_011543464.1:p.Ala767=
XM_011545163.1:c.2290G=	XP_011543465.1:p.Ala764=
XM_011545164.1:c.2281G=	XP_011543466.1:p.Ala761=
XM_011545164.2:c.2281G=	XP_011543466.1:p.Ala761=
NM_018026.4:c.2620G= MANE Select	NP_060496.2:p.Ala874=