Canonical Allele Identifier: CA381383512

Gene: PACS1

Linked Data

• MyVariant Identifiers: chr11:g.66009122A>T (hg19) ; chr11:g.66241651A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66241651A>T , CM000673.2:g.66241651A>T	GRCh38
NC_000011.9:g.66009122A>T , CM000673.1:g.66009122A>T	GRCh37
NC_000011.8:g.65765698A>T	NCBI36
NG_033900.1:g.176299A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.2654A>T MANE Select	ENSP00000316454.4:p.Lys885Ile
ENST00000320580.8:c.2654A>T	ENSP00000316454.4:p.Lys885Ile
ENST00000524815.5:c.38A>T	ENSP00000433991.1:p.Lys13Ile
ENST00000529677.1:c.204A>T
ENST00000529757.5:c.1262A>T	ENSP00000432858.1:p.Lys421Ile
ENST00000531597.1:c.38A>T	ENSP00000434012.1:p.Lys13Ile
NM_018026.3:c.2654A>T	NP_060496.2:p.Lys885Ile
XM_011545162.1:c.2333A>T	XP_011543464.1:p.Lys778Ile
XM_011545163.1:c.2324A>T	XP_011543465.1:p.Lys775Ile
XM_011545164.1:c.2315A>T	XP_011543466.1:p.Lys772Ile
XM_011545164.2:c.2315A>T	XP_011543466.1:p.Lys772Ile
NM_018026.4:c.2654A>T MANE Select	NP_060496.2:p.Lys885Ile