Canonical Allele Identifier: CA945518647
Gene: ABCC9 HGNC NCBI

Linked Data

dbSNP Id: rs1944489897

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21843453_21843454del , CM000674.2:g.21843453_21843454del GRCh38
NC_000012.11:g.21996387_21996388del , CM000674.1:g.21996387_21996388del GRCh37
NC_000012.10:g.21887654_21887655del NCBI36
NG_012819.1:g.98242_98243del , LRG_377:g.98242_98243del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261201.10:c.3316-982_3316-981del ENSP00000261201.4:n.3316-982_3316-981del
ENST00000682068.1:c.3316-982_3316-981del ENSP00000507226.1:n.3316-982_3316-981del
ENST00000682426.1:n.893-982_893-981del
ENST00000682879.1:c.*2414-982_*2414-981del ENSP00000508210.1:n.*2414-982_*2414-981del
ENST00000683105.1:c.3316-982_3316-981del ENSP00000506801.1:n.3316-982_3316-981del
ENST00000683676.1:c.3316-982_3316-981del ENSP00000508167.1:n.3316-982_3316-981del
ENST00000683811.1:n.2817-982_2817-981del
ENST00000684084.1:c.3265-982_3265-981del ENSP00000507859.1:n.3265-982_3265-981del
ENST00000261200.9:c.3316-982_3316-981del MANE Select ENSP00000261200.4:n.3316-982_3316-981del
ENST00000261201.9:c.3316-982_3316-981del ENSP00000261201.4:n.3316-982_3316-981del
ENST00000261200.8:c.3316-982_3316-981del ENSP00000261200.4:n.3316-982_3316-981del
ENST00000261201.8:c.3316-982_3316-981del ENSP00000261201.4:n.3316-982_3316-981del
ENST00000544039.5:c.2197-982_2197-981del ENSP00000440521.1:n.2197-982_2197-981del
NM_005691.3:c.3316-982_3316-981del NP_005682.2:n.3316-982_3316-981del
NM_020297.3:c.3316-982_3316-981del NP_064693.2:n.3316-982_3316-981del
XM_005253284.2:c.3316-982_3316-981del XP_005253341.1:n.3316-982_3316-981del
XM_005253286.2:c.3316-982_3316-981del XP_005253343.1:n.3316-982_3316-981del
XM_005253287.3:c.3316-982_3316-981del XP_005253344.1:n.3316-982_3316-981del
XM_005253288.2:c.3316-982_3316-981del XP_005253345.1:n.3316-982_3316-981del
XM_005253289.2:c.3277-982_3277-981del XP_005253346.1:n.3277-982_3277-981del
XM_005253290.2:c.3175-982_3175-981del XP_005253347.1:n.3175-982_3175-981del
XM_006719025.2:c.3277-982_3277-981del XP_006719088.1:n.3277-982_3277-981del
XM_011520545.1:c.3316-982_3316-981del XP_011518847.1:n.3316-982_3316-981del
XM_005253284.4:c.3316-982_3316-981del XP_005253341.1:n.3316-982_3316-981del
XM_005253286.4:c.3316-982_3316-981del XP_005253343.1:n.3316-982_3316-981del
XM_005253287.5:c.3316-982_3316-981del XP_005253344.1:n.3316-982_3316-981del
XM_005253288.4:c.3316-982_3316-981del XP_005253345.1:n.3316-982_3316-981del
XM_005253289.4:c.3277-982_3277-981del XP_005253346.1:n.3277-982_3277-981del
XM_005253290.4:c.3175-982_3175-981del XP_005253347.1:n.3175-982_3175-981del
XM_006719025.4:c.3277-982_3277-981del XP_006719088.1:n.3277-982_3277-981del
XM_011520545.3:c.3316-982_3316-981del XP_011518847.1:n.3316-982_3316-981del
NM_001377273.1:c.3316-982_3316-981del NP_001364202.1:n.3316-982_3316-981del
NM_001377274.1:c.2449-982_2449-981del NP_001364203.1:n.2449-982_2449-981del
NM_005691.4:c.3316-982_3316-981del NP_005682.2:n.3316-982_3316-981del
NM_020297.4:c.3316-982_3316-981del MANE Select NP_064693.2:n.3316-982_3316-981del