Canonical Allele Identifier: CA2614443911

Gene: PACS1

Linked Data

• gnomAD v4: 11-66211113-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66211116_66211117del , CM000673.2:g.66211116_66211117del	GRCh38
NC_000011.9:g.65978587_65978588del , CM000673.1:g.65978587_65978588del	GRCh37
NC_000011.8:g.65735163_65735164del	NCBI36
NG_033900.1:g.145764_145765del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.535-18_535-17del MANE Select	ENSP00000316454.4:n.535-18_535-17del
ENST00000320580.8:c.535-18_535-17del	ENSP00000316454.4:n.535-18_535-17del
ENST00000527224.1:n.659-18_659-17del
ENST00000527380.1:c.241-18_241-17del	ENSP00000432639.1:n.241-18_241-17del
ENST00000533756.5:c.226-18_226-17del	ENSP00000437150.1:n.226-18_226-17del
NM_018026.3:c.535-18_535-17del	NP_060496.2:n.535-18_535-17del
XM_011545162.1:c.214-18_214-17del	XP_011543464.1:n.214-18_214-17del
XM_011545163.1:c.205-18_205-17del	XP_011543465.1:n.205-18_205-17del
XM_011545164.1:c.196-18_196-17del	XP_011543466.1:n.196-18_196-17del
XM_011545164.2:c.196-18_196-17del	XP_011543466.1:n.196-18_196-17del
XR_001747924.1:n.746-18_746-17del
NM_018026.4:c.535-18_535-17del MANE Select	NP_060496.2:n.535-18_535-17del