Canonical Allele Identifier: CA640741701
Gene: AP1S2 HGNC NCBI

Linked Data

dbSNP Id: rs1371913647

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.15851975del , CM000685.2:g.15851975del GRCh38
NC_000023.10:g.15870098del , CM000685.1:g.15870098del GRCh37
NC_000023.9:g.15780019del NCBI36
NG_009274.1:g.8007del
NG_009274.2:g.8007del

Transcript Alleles

HGVS Amino-acid Change
ENST00000450644.2:c.179+375del ENSP00000389474.2:n.179+375del
ENST00000479184.2:c.179+375del ENSP00000500850.1:n.179+375del
ENST00000545766.7:c.47+375del ENSP00000444957.3:n.47+375del
ENST00000671830.1:c.179+375del ENSP00000500483.1:n.179+375del
ENST00000672063.1:c.179+375del ENSP00000500737.1:n.179+375del
ENST00000672987.1:c.179+375del MANE Select ENSP00000500695.1:n.179+375del
ENST00000673445.1:c.179+375del ENSP00000500798.1:n.179+375del
ENST00000673591.1:c.179+375del ENSP00000500066.1:n.179+375del
ENST00000329235.6:c.179+375del ENSP00000328789.2:n.179+375del
ENST00000380291.5:c.179+375del ENSP00000369645.1:n.179+375del
ENST00000450644.1:c.157+375del
ENST00000452376.5:c.168+375del
ENST00000545766.5:c.179+375del ENSP00000444957.2:n.179+375del
NM_001272071.1:c.179+375del NP_001259000.1:n.179+375del
NM_003916.4:c.179+375del NP_003907.3:n.179+375del
XM_005274614.3:c.305+375del XP_005274671.1:n.305+375del
XM_011545599.1:c.305+375del XP_011543901.1:n.305+375del
XR_247289.2:n.458+375del
XR_247290.3:n.393+375del
XM_017029925.1:c.305+375del XP_016885414.1:n.305+375del
XM_017029926.2:c.305+375del XP_016885415.1:n.305+375del
XR_001755741.2:n.458+375del
XR_002958809.1:n.229+375del
XR_247289.3:n.458+375del
XR_247290.4:n.458+375del
NM_001272071.2:c.179+375del MANE Select NP_001259000.1:n.179+375del
NM_001368994.1:c.179+375del NP_001355923.1:n.179+375del
NM_001369007.1:c.179+375del NP_001355936.1:n.179+375del
NM_001369008.1:c.179+375del NP_001355937.1:n.179+375del
NM_003916.5:c.179+375del NP_003907.3:n.179+375del
NR_160932.1:n.305+375del
NR_160933.1:n.305+375del