Canonical Allele Identifier: CA381383106

Gene: PACS1

Linked Data

• MyVariant Identifiers: chr11:g.66009077C>A (hg19) ; chr11:g.66241606C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66241606C>A , CM000673.2:g.66241606C>A	GRCh38
NC_000011.9:g.66009077C>A , CM000673.1:g.66009077C>A	GRCh37
NC_000011.8:g.65765653C>A	NCBI36
NG_033900.1:g.176254C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.2609C>A MANE Select	ENSP00000316454.4:p.Ser870Tyr
ENST00000320580.8:c.2609C>A	ENSP00000316454.4:p.Ser870Tyr
ENST00000524815.5:c.-8C>A	ENSP00000433991.1:n.-8C>A
ENST00000529677.1:c.159C>A
ENST00000529757.5:c.1217C>A	ENSP00000432858.1:p.Ser406Tyr
ENST00000531597.1:c.-8C>A	ENSP00000434012.1:n.-8C>A
NM_018026.3:c.2609C>A	NP_060496.2:p.Ser870Tyr
XM_011545162.1:c.2288C>A	XP_011543464.1:p.Ser763Tyr
XM_011545163.1:c.2279C>A	XP_011543465.1:p.Ser760Tyr
XM_011545164.1:c.2270C>A	XP_011543466.1:p.Ser757Tyr
XM_011545164.2:c.2270C>A	XP_011543466.1:p.Ser757Tyr
NM_018026.4:c.2609C>A MANE Select	NP_060496.2:p.Ser870Tyr