Canonical Allele Identifier: CA1979644237

Gene: PACS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66242012_66242015delinsCAGG , CM000673.2:g.66242012_66242015delinsCAGG	GRCh38
NC_000011.9:g.66009483_66009486delinsCAGG , CM000673.1:g.66009483_66009486delinsCAGG	GRCh37
NC_000011.8:g.65766059_65766062delinsCAGG	NCBI36
NG_033900.1:g.176660_176663delinsCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.2656+359_2656+362delinsCAGG MANE Select	ENSP00000316454.4:n.2656+359_2656+362delinsCAGG
ENST00000320580.8:c.2656+359_2656+362delinsCAGG	ENSP00000316454.4:n.2656+359_2656+362delinsCAGG
ENST00000524815.5:c.40+359_40+362delinsCAGG	ENSP00000433991.1:n.40+359_40+362delinsCAGG
ENST00000529677.1:c.206+359_206+362delinsCAGG
ENST00000529757.5:c.1264+359_1264+362delinsCAGG	ENSP00000432858.1:n.1264+359_1264+362delinsCAGG
ENST00000531597.1:c.40+359_40+362delinsCAGG	ENSP00000434012.1:n.40+359_40+362delinsCAGG
NM_018026.3:c.2656+359_2656+362delinsCAGG	NP_060496.2:n.2656+359_2656+362delinsCAGG
XM_011545162.1:c.2335+359_2335+362delinsCAGG	XP_011543464.1:n.2335+359_2335+362delinsCAGG
XM_011545163.1:c.2326+359_2326+362delinsCAGG	XP_011543465.1:n.2326+359_2326+362delinsCAGG
XM_011545164.1:c.2317+359_2317+362delinsCAGG	XP_011543466.1:n.2317+359_2317+362delinsCAGG
XM_011545164.2:c.2317+359_2317+362delinsCAGG	XP_011543466.1:n.2317+359_2317+362delinsCAGG
NM_018026.4:c.2656+359_2656+362delinsCAGG MANE Select	NP_060496.2:n.2656+359_2656+362delinsCAGG