Canonical Allele Identifier: CA233611514
Gene: ABCC9 HGNC NCBI

Linked Data

dbSNP Id: rs371525457

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21872721dup , CM000674.2:g.21872721dup GRCh38
NC_000012.11:g.22025655dup , CM000674.1:g.22025655dup GRCh37
NC_000012.10:g.21916922dup NCBI36
NG_012819.1:g.68975dup , LRG_377:g.68975dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261201.10:c.2103dup ENSP00000261201.4:p.Met702HisfsTer20
ENST00000682068.1:c.2103dup ENSP00000507226.1:p.Met702HisfsTer20
ENST00000682879.1:c.*1204dup ENSP00000508210.1:n.*1204dup
ENST00000683105.1:c.2103dup ENSP00000506801.1:p.Met702HisfsTer20
ENST00000683676.1:c.2103dup ENSP00000508167.1:p.Met702HisfsTer20
ENST00000684084.1:c.2103dup ENSP00000507859.1:p.Met702HisfsTer20
ENST00000684543.1:n.2448dup
ENST00000261200.9:c.2103dup MANE Select ENSP00000261200.4:p.Met702HisfsTer20
ENST00000261201.9:c.2103dup ENSP00000261201.4:p.Met702HisfsTer20
ENST00000261200.8:c.2103dup ENSP00000261200.4:p.Met702HisfsTer20
ENST00000261201.8:c.2103dup ENSP00000261201.4:p.Met702HisfsTer20
ENST00000544039.5:c.984dup ENSP00000440521.1:p.Met329HisfsTer20
NM_005691.3:c.2103dup NP_005682.2:p.Met702HisfsTer20
NM_020297.3:c.2103dup NP_064693.2:p.Met702HisfsTer20
XM_005253284.2:c.2103dup XP_005253341.1:p.Met702HisfsTer20
XM_005253286.2:c.2103dup XP_005253343.1:p.Met702HisfsTer20
XM_005253287.3:c.2103dup XP_005253344.1:p.Met702HisfsTer20
XM_005253288.2:c.2103dup XP_005253345.1:p.Met702HisfsTer20
XM_005253289.2:c.2103dup XP_005253346.1:p.Met702HisfsTer20
XM_005253290.2:c.2103dup XP_005253347.1:p.Met702HisfsTer20
XM_006719025.2:c.2103dup XP_006719088.1:p.Met702HisfsTer20
XM_011520545.1:c.2103dup XP_011518847.1:p.Met702HisfsTer20
XM_005253284.4:c.2103dup XP_005253341.1:p.Met702HisfsTer20
XM_005253286.4:c.2103dup XP_005253343.1:p.Met702HisfsTer20
XM_005253287.5:c.2103dup XP_005253344.1:p.Met702HisfsTer20
XM_005253288.4:c.2103dup XP_005253345.1:p.Met702HisfsTer20
XM_005253289.4:c.2103dup XP_005253346.1:p.Met702HisfsTer20
XM_005253290.4:c.2103dup XP_005253347.1:p.Met702HisfsTer20
XM_006719025.4:c.2103dup XP_006719088.1:p.Met702HisfsTer20
XM_011520545.3:c.2103dup XP_011518847.1:p.Met702HisfsTer20
NM_001377273.1:c.2103dup NP_001364202.1:p.Met702HisfsTer20
NM_001377274.1:c.1239dup NP_001364203.1:p.Met414HisfsTer20
NM_005691.4:c.2103dup NP_005682.2:p.Met702HisfsTer20
NM_020297.4:c.2103dup MANE Select NP_064693.2:p.Met702HisfsTer20