Canonical Allele Identifier: CA475300430

Gene: PACS1

Linked Data

• MyVariant Identifiers: chr11:g.65978685C>A (hg19)

Genomic Alleles

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

Transcript Alleles

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