Canonical Allele Identifier: CA679383045

Gene: PACS1

Linked Data

• dbSNP Id: rs1374993883
• gnomAD v3: 11-66211109-C-T
• gnomAD v4: 11-66211109-C-T
• MyVariant Identifiers: chr11:g.65978580C>T (hg19) ; chr11:g.66211109C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66211109C>T , CM000673.2:g.66211109C>T	GRCh38
NC_000011.9:g.65978580C>T , CM000673.1:g.65978580C>T	GRCh37
NC_000011.8:g.65735156C>T	NCBI36
NG_033900.1:g.145757C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.535-25C>T MANE Select	ENSP00000316454.4:n.535-25C>T
ENST00000320580.8:c.535-25C>T	ENSP00000316454.4:n.535-25C>T
ENST00000527224.1:n.659-25C>T
ENST00000527380.1:c.241-25C>T	ENSP00000432639.1:n.241-25C>T
ENST00000533756.5:c.226-25C>T	ENSP00000437150.1:n.226-25C>T
NM_018026.3:c.535-25C>T	NP_060496.2:n.535-25C>T
XM_011545162.1:c.214-25C>T	XP_011543464.1:n.214-25C>T
XM_011545163.1:c.205-25C>T	XP_011543465.1:n.205-25C>T
XM_011545164.1:c.196-25C>T	XP_011543466.1:n.196-25C>T
XM_011545164.2:c.196-25C>T	XP_011543466.1:n.196-25C>T
XR_001747924.1:n.746-25C>T
NM_018026.4:c.535-25C>T MANE Select	NP_060496.2:n.535-25C>T