Canonical Allele Identifier: CA1979579383
Gene: PACS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66211214C= , CM000673.2:g.66211214C= GRCh38
NC_000011.9:g.65978685C= , CM000673.1:g.65978685C= GRCh37
NC_000011.8:g.65735261C= NCBI36
NG_033900.1:g.145862C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320580.9:c.615C= MANE Select ENSP00000316454.4:p.Ile205=
ENST00000320580.8:c.615C= ENSP00000316454.4:p.Ile205=
ENST00000527224.1:n.739C=
ENST00000527380.1:c.321C= ENSP00000432639.1:p.Ile107=
ENST00000533756.5:c.306C= ENSP00000437150.1:p.Ile102=
NM_018026.3:c.615C= NP_060496.2:p.Ile205=
XM_011545162.1:c.294C= XP_011543464.1:p.Ile98=
XM_011545163.1:c.285C= XP_011543465.1:p.Ile95=
XM_011545164.1:c.276C= XP_011543466.1:p.Ile92=
XM_011545164.2:c.276C= XP_011543466.1:p.Ile92=
XR_001747924.1:n.826C=
NM_018026.4:c.615C= MANE Select NP_060496.2:p.Ile205=