Canonical Allele Identifier: CA2021322301
Gene: ABCC9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21889267_21889271delinsACTTT , CM000674.2:g.21889267_21889271delinsACTTT GRCh38
NC_000012.11:g.22042201_22042205delinsACTTT , CM000674.1:g.22042201_22042205delinsACTTT GRCh37
NC_000012.10:g.21933468_21933472delinsACTTT NCBI36
NG_012819.1:g.52424_52428delinsAAAGT , LRG_377:g.52424_52428delinsAAAGT

Transcript Alleles

HGVS Amino-acid change
ENST00000261201.10:c.1803-1337_1803-1333delinsAAAGT ENSP00000261201.4:n.1803-1337_1803-1333de...
ENST00000682068.1:c.1803-1337_1803-1333delinsAAAGT ENSP00000507226.1:n.1803-1337_1803-1333de...
ENST00000682789.1:n.2054-1337_2054-1333delinsAAAGT
ENST00000682879.1:c.*904-1337_*904-1333delinsAAAGT ENSP00000508210.1:n.*904-1337_*904-1333de...
ENST00000683105.1:c.1803-1337_1803-1333delinsAAAGT ENSP00000506801.1:n.1803-1337_1803-1333de...
ENST00000683676.1:c.1803-1337_1803-1333delinsAAAGT ENSP00000508167.1:n.1803-1337_1803-1333de...
ENST00000684084.1:c.1803-1337_1803-1333delinsAAAGT ENSP00000507859.1:n.1803-1337_1803-1333de...
ENST00000684543.1:n.2148-1337_2148-1333delinsAAAGT
ENST00000261200.9:c.1803-1337_1803-1333delinsAAAGT MANE Select ENSP00000261200.4:n.1803-1337_1803-1333de...
ENST00000261201.9:c.1803-1337_1803-1333delinsAAAGT ENSP00000261201.4:n.1803-1337_1803-1333de...
ENST00000261200.8:c.1803-1337_1803-1333delinsAAAGT ENSP00000261200.4:n.1803-1337_1803-1333de...
ENST00000261201.8:c.1803-1337_1803-1333delinsAAAGT ENSP00000261201.4:n.1803-1337_1803-1333de...
ENST00000544039.5:c.792-1337_792-1333delinsAAAGT ENSP00000440521.1:n.792-1337_792-1333deli...
NM_005691.3:c.1803-1337_1803-1333delinsAAAGT NP_005682.2:n.1803-1337_1803-1333delinsAA...
NM_020297.3:c.1803-1337_1803-1333delinsAAAGT NP_064693.2:n.1803-1337_1803-1333delinsAA...
XM_005253284.2:c.1803-1337_1803-1333delinsAAAGT XP_005253341.1:n.1803-1337_1803-1333delin...
XM_005253286.2:c.1803-1337_1803-1333delinsAAAGT XP_005253343.1:n.1803-1337_1803-1333delin...
XM_005253287.3:c.1803-1337_1803-1333delinsAAAGT XP_005253344.1:n.1803-1337_1803-1333delin...
XM_005253288.2:c.1803-1337_1803-1333delinsAAAGT XP_005253345.1:n.1803-1337_1803-1333delin...
XM_005253289.2:c.1803-1337_1803-1333delinsAAAGT XP_005253346.1:n.1803-1337_1803-1333delin...
XM_005253290.2:c.1803-1337_1803-1333delinsAAAGT XP_005253347.1:n.1803-1337_1803-1333delin...
XM_006719025.2:c.1803-1337_1803-1333delinsAAAGT XP_006719088.1:n.1803-1337_1803-1333delin...
XM_011520545.1:c.1803-1337_1803-1333delinsAAAGT XP_011518847.1:n.1803-1337_1803-1333delin...
XM_005253284.4:c.1803-1337_1803-1333delinsAAAGT XP_005253341.1:n.1803-1337_1803-1333delin...
XM_005253286.4:c.1803-1337_1803-1333delinsAAAGT XP_005253343.1:n.1803-1337_1803-1333delin...
XM_005253287.5:c.1803-1337_1803-1333delinsAAAGT XP_005253344.1:n.1803-1337_1803-1333delin...
XM_005253288.4:c.1803-1337_1803-1333delinsAAAGT XP_005253345.1:n.1803-1337_1803-1333delin...
XM_005253289.4:c.1803-1337_1803-1333delinsAAAGT XP_005253346.1:n.1803-1337_1803-1333delin...
XM_005253290.4:c.1803-1337_1803-1333delinsAAAGT XP_005253347.1:n.1803-1337_1803-1333delin...
XM_006719025.4:c.1803-1337_1803-1333delinsAAAGT XP_006719088.1:n.1803-1337_1803-1333delin...
XM_011520545.3:c.1803-1337_1803-1333delinsAAAGT XP_011518847.1:n.1803-1337_1803-1333delin...
NM_001377273.1:c.1803-1337_1803-1333delinsAAAGT NP_001364202.1:n.1803-1337_1803-1333delin...
NM_001377274.1:c.939-1337_939-1333delinsAAAGT NP_001364203.1:n.939-1337_939-1333delinsA...
NM_005691.4:c.1803-1337_1803-1333delinsAAAGT NP_005682.2:n.1803-1337_1803-1333delinsAA...
NM_020297.4:c.1803-1337_1803-1333delinsAAAGT MANE Select NP_064693.2:n.1803-1337_1803-1333delinsAA...