Canonical Allele Identifier: CA679383054

Gene: PACS1

Linked Data

• dbSNP Id: rs1381670510
• gnomAD v4: 11-66211125-A-G
• MyVariant Identifiers: chr11:g.65978596A>G (hg19) ; chr11:g.66211125A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66211125A>G , CM000673.2:g.66211125A>G	GRCh38
NC_000011.9:g.65978596A>G , CM000673.1:g.65978596A>G	GRCh37
NC_000011.8:g.65735172A>G	NCBI36
NG_033900.1:g.145773A>G

Transcript Alleles

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