Canonical Allele Identifier: CA475300513

Gene: PACS1

Linked Data

• gnomAD v4: 11-66211220-C-G
• MyVariant Identifiers: chr11:g.65978691C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66211220C>G , CM000673.2:g.66211220C>G	GRCh38
NC_000011.9:g.65978691C>G , CM000673.1:g.65978691C>G	GRCh37
NC_000011.8:g.65735267C>G	NCBI36
NG_033900.1:g.145868C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.621C>G MANE Select	ENSP00000316454.4:p.Gly207=
ENST00000320580.8:c.621C>G	ENSP00000316454.4:p.Gly207=
ENST00000527224.1:n.745C>G
ENST00000527380.1:c.327C>G	ENSP00000432639.1:p.Gly109=
ENST00000533756.5:c.312C>G	ENSP00000437150.1:p.Gly104=
NM_018026.3:c.621C>G	NP_060496.2:p.Gly207=
XM_011545162.1:c.300C>G	XP_011543464.1:p.Gly100=
XM_011545163.1:c.291C>G	XP_011543465.1:p.Gly97=
XM_011545164.1:c.282C>G	XP_011543466.1:p.Gly94=
XM_011545164.2:c.282C>G	XP_011543466.1:p.Gly94=
XR_001747924.1:n.832C>G
NM_018026.4:c.621C>G MANE Select	NP_060496.2:p.Gly207=