Canonical Allele Identifier: CA381342525

Gene: PACS1

Linked Data

• MyVariant Identifiers: chr11:g.65978683A>G (hg19) ; chr11:g.66211212A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66211212A>G , CM000673.2:g.66211212A>G	GRCh38
NC_000011.9:g.65978683A>G , CM000673.1:g.65978683A>G	GRCh37
NC_000011.8:g.65735259A>G	NCBI36
NG_033900.1:g.145860A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.613A>G MANE Select	ENSP00000316454.4:p.Ile205Val
ENST00000320580.8:c.613A>G	ENSP00000316454.4:p.Ile205Val
ENST00000527224.1:n.737A>G
ENST00000527380.1:c.319A>G	ENSP00000432639.1:p.Ile107Val
ENST00000533756.5:c.304A>G	ENSP00000437150.1:p.Ile102Val
NM_018026.3:c.613A>G	NP_060496.2:p.Ile205Val
XM_011545162.1:c.292A>G	XP_011543464.1:p.Ile98Val
XM_011545163.1:c.283A>G	XP_011543465.1:p.Ile95Val
XM_011545164.1:c.274A>G	XP_011543466.1:p.Ile92Val
XM_011545164.2:c.274A>G	XP_011543466.1:p.Ile92Val
XR_001747924.1:n.824A>G
NM_018026.4:c.613A>G MANE Select	NP_060496.2:p.Ile205Val