Canonical Allele Identifier: CA679383050

Gene: PACS1

Linked Data

• dbSNP Id: rs1301666148
• gnomAD v3: 11-66211115-T-A
• gnomAD v4: 11-66211115-T-A
• MyVariant Identifiers: chr11:g.65978586T>A (hg19) ; chr11:g.66211115T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66211115T>A , CM000673.2:g.66211115T>A	GRCh38
NC_000011.9:g.65978586T>A , CM000673.1:g.65978586T>A	GRCh37
NC_000011.8:g.65735162T>A	NCBI36
NG_033900.1:g.145763T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.535-19T>A MANE Select	ENSP00000316454.4:n.535-19T>A
ENST00000320580.8:c.535-19T>A	ENSP00000316454.4:n.535-19T>A
ENST00000527224.1:n.659-19T>A
ENST00000527380.1:c.241-19T>A	ENSP00000432639.1:n.241-19T>A
ENST00000533756.5:c.226-19T>A	ENSP00000437150.1:n.226-19T>A
NM_018026.3:c.535-19T>A	NP_060496.2:n.535-19T>A
XM_011545162.1:c.214-19T>A	XP_011543464.1:n.214-19T>A
XM_011545163.1:c.205-19T>A	XP_011543465.1:n.205-19T>A
XM_011545164.1:c.196-19T>A	XP_011543466.1:n.196-19T>A
XM_011545164.2:c.196-19T>A	XP_011543466.1:n.196-19T>A
XR_001747924.1:n.746-19T>A
NM_018026.4:c.535-19T>A MANE Select	NP_060496.2:n.535-19T>A