Canonical Allele Identifier: CA2021333479
Gene: ABCC9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21917233_21917235delinsGGT , CM000674.2:g.21917233_21917235delinsGGT GRCh38
NC_000012.11:g.22070167_22070169delinsGGT , CM000674.1:g.22070167_22070169delinsGGT GRCh37
NC_000012.10:g.21961434_21961436delinsGGT NCBI36
NG_012819.1:g.24460_24462delinsACC , LRG_377:g.24460_24462delinsACC

Transcript Alleles

HGVS Amino-acid change
ENST00000261201.10:c.407-132_407-130delinsACC ENSP00000261201.4:n.407-132_407-130delins...
ENST00000682068.1:c.407-132_407-130delinsACC ENSP00000507226.1:n.407-132_407-130delins...
ENST00000682789.1:n.658-132_658-130delinsACC
ENST00000682879.1:c.407-4169_407-4167delinsACC ENSP00000508210.1:n.407-4169_407-4167deli...
ENST00000683105.1:c.407-132_407-130delinsACC ENSP00000506801.1:n.407-132_407-130delins...
ENST00000683676.1:c.407-132_407-130delinsACC ENSP00000508167.1:n.407-132_407-130delins...
ENST00000684084.1:c.407-132_407-130delinsACC ENSP00000507859.1:n.407-132_407-130delins...
ENST00000684543.1:n.752-132_752-130delinsACC
ENST00000261200.9:c.407-132_407-130delinsACC MANE Select ENSP00000261200.4:n.407-132_407-130delins...
ENST00000261201.9:c.407-132_407-130delinsACC ENSP00000261201.4:n.407-132_407-130delins...
ENST00000261200.8:c.407-132_407-130delinsACC ENSP00000261200.4:n.407-132_407-130delins...
ENST00000261201.8:c.407-132_407-130delinsACC ENSP00000261201.4:n.407-132_407-130delins...
NM_005691.3:c.407-132_407-130delinsACC NP_005682.2:n.407-132_407-130delinsACC
NM_020297.3:c.407-132_407-130delinsACC NP_064693.2:n.407-132_407-130delinsACC
XM_005253284.2:c.407-132_407-130delinsACC XP_005253341.1:n.407-132_407-130delinsACC...
XM_005253286.2:c.407-132_407-130delinsACC XP_005253343.1:n.407-132_407-130delinsACC...
XM_005253287.3:c.407-132_407-130delinsACC XP_005253344.1:n.407-132_407-130delinsACC...
XM_005253288.2:c.407-132_407-130delinsACC XP_005253345.1:n.407-132_407-130delinsACC...
XM_005253289.2:c.407-132_407-130delinsACC XP_005253346.1:n.407-132_407-130delinsACC...
XM_005253290.2:c.407-132_407-130delinsACC XP_005253347.1:n.407-132_407-130delinsACC...
XM_006719025.2:c.407-132_407-130delinsACC XP_006719088.1:n.407-132_407-130delinsACC...
XM_011520545.1:c.407-132_407-130delinsACC XP_011518847.1:n.407-132_407-130delinsACC...
XM_005253284.4:c.407-132_407-130delinsACC XP_005253341.1:n.407-132_407-130delinsACC...
XM_005253286.4:c.407-132_407-130delinsACC XP_005253343.1:n.407-132_407-130delinsACC...
XM_005253287.5:c.407-132_407-130delinsACC XP_005253344.1:n.407-132_407-130delinsACC...
XM_005253288.4:c.407-132_407-130delinsACC XP_005253345.1:n.407-132_407-130delinsACC...
XM_005253289.4:c.407-132_407-130delinsACC XP_005253346.1:n.407-132_407-130delinsACC...
XM_005253290.4:c.407-132_407-130delinsACC XP_005253347.1:n.407-132_407-130delinsACC...
XM_006719025.4:c.407-132_407-130delinsACC XP_006719088.1:n.407-132_407-130delinsACC...
XM_011520545.3:c.407-132_407-130delinsACC XP_011518847.1:n.407-132_407-130delinsACC...
NM_001377273.1:c.407-132_407-130delinsACC NP_001364202.1:n.407-132_407-130delinsACC...
NM_001377274.1:c.-48-4169_-48-4167delinsACC NP_001364203.1:n.-48-4169_-48-4167delinsA...
NM_005691.4:c.407-132_407-130delinsACC NP_005682.2:n.407-132_407-130delinsACC
NM_020297.4:c.407-132_407-130delinsACC MANE Select NP_064693.2:n.407-132_407-130delinsACC