Canonical Allele Identifier: CA224025412
Community Standard Title: NM_018026.4(PACS1):c.445-300T>G
Gene: PACS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66210062T>G , CM000673.2:g.66210062T>G GRCh38
NC_000011.9:g.65977533T>G , CM000673.1:g.65977533T>G GRCh37
NC_000011.8:g.65734109T>G NCBI36
NG_033900.1:g.144710T>G

Transcript Alleles

HGVS Amino-acid Change
NM_018026.4:c.445-300T>G MANE Select NP_060496.2:n.445-300T>G
ENST00000320580.9:c.445-300T>G MANE Select ENSP00000316454.4:n.445-300T>G
NM_018026.3:c.445-300T>G NP_060496.2:n.445-300T>G
ENST00000320580.8:c.445-300T>G ENSP00000316454.4:n.445-300T>G
ENST00000527224.1:n.569-300T>G
ENST00000527380.1:c.151-300T>G ENSP00000432639.1:n.151-300T>G
ENST00000533756.5:c.136-300T>G ENSP00000437150.1:n.136-300T>G
XM_011545162.1:c.124-300T>G XP_011543464.1:n.124-300T>G
XM_011545163.1:c.115-300T>G XP_011543465.1:n.115-300T>G
XM_011545164.1:c.106-300T>G XP_011543466.1:n.106-300T>G
XM_011545164.2:c.106-300T>G XP_011543466.1:n.106-300T>G
XR_001747924.1:n.656-300T>G