Canonical Allele Identifier: CA1979579260

Gene: PACS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66211116_66211118delinsCTG , CM000673.2:g.66211116_66211118delinsCTG	GRCh38
NC_000011.9:g.65978587_65978589delinsCTG , CM000673.1:g.65978587_65978589delinsCTG	GRCh37
NC_000011.8:g.65735163_65735165delinsCTG	NCBI36
NG_033900.1:g.145764_145766delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.535-18_535-16delinsCTG MANE Select	ENSP00000316454.4:n.535-18_535-16delinsCTG
ENST00000320580.8:c.535-18_535-16delinsCTG	ENSP00000316454.4:n.535-18_535-16delinsCTG
ENST00000527224.1:n.659-18_659-16delinsCTG
ENST00000527380.1:c.241-18_241-16delinsCTG	ENSP00000432639.1:n.241-18_241-16delinsCTG
ENST00000533756.5:c.226-18_226-16delinsCTG	ENSP00000437150.1:n.226-18_226-16delinsCTG
NM_018026.3:c.535-18_535-16delinsCTG	NP_060496.2:n.535-18_535-16delinsCTG
XM_011545162.1:c.214-18_214-16delinsCTG	XP_011543464.1:n.214-18_214-16delinsCTG
XM_011545163.1:c.205-18_205-16delinsCTG	XP_011543465.1:n.205-18_205-16delinsCTG
XM_011545164.1:c.196-18_196-16delinsCTG	XP_011543466.1:n.196-18_196-16delinsCTG
XM_011545164.2:c.196-18_196-16delinsCTG	XP_011543466.1:n.196-18_196-16delinsCTG
XR_001747924.1:n.746-18_746-16delinsCTG
NM_018026.4:c.535-18_535-16delinsCTG MANE Select	NP_060496.2:n.535-18_535-16delinsCTG