Canonical Allele Identifier: CA381382765

Gene: PACS1

Linked Data

• MyVariant Identifiers: chr11:g.66009046C>T (hg19) ; chr11:g.66241575C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66241575C>T , CM000673.2:g.66241575C>T	GRCh38
NC_000011.9:g.66009046C>T , CM000673.1:g.66009046C>T	GRCh37
NC_000011.8:g.65765622C>T	NCBI36
NG_033900.1:g.176223C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.2578C>T MANE Select	ENSP00000316454.4:p.Arg860Cys
ENST00000320580.8:c.2578C>T	ENSP00000316454.4:p.Arg860Cys
ENST00000524815.5:c.-39C>T	ENSP00000433991.1:n.-39C>T
ENST00000529677.1:c.128C>T
ENST00000529757.5:c.1186C>T	ENSP00000432858.1:p.Arg396Cys
ENST00000531597.1:c.-39C>T	ENSP00000434012.1:n.-39C>T
NM_018026.3:c.2578C>T	NP_060496.2:p.Arg860Cys
XM_011545162.1:c.2257C>T	XP_011543464.1:p.Arg753Cys
XM_011545163.1:c.2248C>T	XP_011543465.1:p.Arg750Cys
XM_011545164.1:c.2239C>T	XP_011543466.1:p.Arg747Cys
XM_011545164.2:c.2239C>T	XP_011543466.1:p.Arg747Cys
NM_018026.4:c.2578C>T MANE Select	NP_060496.2:p.Arg860Cys