Canonical Allele Identifier: CA1979644120

Gene: PACS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66241786_66241787delinsAG , CM000673.2:g.66241786_66241787delinsAG	GRCh38
NC_000011.9:g.66009257_66009258delinsAG , CM000673.1:g.66009257_66009258delinsAG	GRCh37
NC_000011.8:g.65765833_65765834delinsAG	NCBI36
NG_033900.1:g.176434_176435delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.2656+133_2656+134delinsAG MANE Select	ENSP00000316454.4:n.2656+133_2656+134delinsAG
ENST00000320580.8:c.2656+133_2656+134delinsAG	ENSP00000316454.4:n.2656+133_2656+134delinsAG
ENST00000524815.5:c.40+133_40+134delinsAG	ENSP00000433991.1:n.40+133_40+134delinsAG
ENST00000529677.1:c.206+133_206+134delinsAG
ENST00000529757.5:c.1264+133_1264+134delinsAG	ENSP00000432858.1:n.1264+133_1264+134delinsAG
ENST00000531597.1:c.40+133_40+134delinsAG	ENSP00000434012.1:n.40+133_40+134delinsAG
NM_018026.3:c.2656+133_2656+134delinsAG	NP_060496.2:n.2656+133_2656+134delinsAG
XM_011545162.1:c.2335+133_2335+134delinsAG	XP_011543464.1:n.2335+133_2335+134delinsAG
XM_011545163.1:c.2326+133_2326+134delinsAG	XP_011543465.1:n.2326+133_2326+134delinsAG
XM_011545164.1:c.2317+133_2317+134delinsAG	XP_011543466.1:n.2317+133_2317+134delinsAG
XM_011545164.2:c.2317+133_2317+134delinsAG	XP_011543466.1:n.2317+133_2317+134delinsAG
NM_018026.4:c.2656+133_2656+134delinsAG MANE Select	NP_060496.2:n.2656+133_2656+134delinsAG