Canonical Allele Identifier: CA381342592

Gene: PACS1

Linked Data

• MyVariant Identifiers: chr11:g.65978689G>A (hg19) ; chr11:g.66211218G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66211218G>A , CM000673.2:g.66211218G>A	GRCh38
NC_000011.9:g.65978689G>A , CM000673.1:g.65978689G>A	GRCh37
NC_000011.8:g.65735265G>A	NCBI36
NG_033900.1:g.145866G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.619G>A MANE Select	ENSP00000316454.4:p.Gly207Ser
ENST00000320580.8:c.619G>A	ENSP00000316454.4:p.Gly207Ser
ENST00000527224.1:n.743G>A
ENST00000527380.1:c.325G>A	ENSP00000432639.1:p.Gly109Ser
ENST00000533756.5:c.310G>A	ENSP00000437150.1:p.Gly104Ser
NM_018026.3:c.619G>A	NP_060496.2:p.Gly207Ser
XM_011545162.1:c.298G>A	XP_011543464.1:p.Gly100Ser
XM_011545163.1:c.289G>A	XP_011543465.1:p.Gly97Ser
XM_011545164.1:c.280G>A	XP_011543466.1:p.Gly94Ser
XM_011545164.2:c.280G>A	XP_011543466.1:p.Gly94Ser
XR_001747924.1:n.830G>A
NM_018026.4:c.619G>A MANE Select	NP_060496.2:p.Gly207Ser