Canonical Allele Identifier: CA381342398

Gene: PACS1

Linked Data

• MyVariant Identifiers: chr11:g.65978677C>G (hg19) ; chr11:g.66211206C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66211206C>G , CM000673.2:g.66211206C>G	GRCh38
NC_000011.9:g.65978677C>G , CM000673.1:g.65978677C>G	GRCh37
NC_000011.8:g.65735253C>G	NCBI36
NG_033900.1:g.145854C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.607C>G MANE Select	ENSP00000316454.4:p.Arg203Gly
ENST00000320580.8:c.607C>G	ENSP00000316454.4:p.Arg203Gly
ENST00000527224.1:n.731C>G
ENST00000527380.1:c.313C>G	ENSP00000432639.1:p.Arg105Gly
ENST00000533756.5:c.298C>G	ENSP00000437150.1:p.Arg100Gly
NM_018026.3:c.607C>G	NP_060496.2:p.Arg203Gly
XM_011545162.1:c.286C>G	XP_011543464.1:p.Arg96Gly
XM_011545163.1:c.277C>G	XP_011543465.1:p.Arg93Gly
XM_011545164.1:c.268C>G	XP_011543466.1:p.Arg90Gly
XM_011545164.2:c.268C>G	XP_011543466.1:p.Arg90Gly
XR_001747924.1:n.818C>G
NM_018026.4:c.607C>G MANE Select	NP_060496.2:p.Arg203Gly