Canonical Allele Identifier: CA2021290880
Gene: ABCC9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21805351A= , CM000674.2:g.21805351A= GRCh38
NC_000012.11:g.21958285A= , CM000674.1:g.21958285A= GRCh37
NC_000012.10:g.21849552A= NCBI36
NG_012819.1:g.136344T= , LRG_377:g.136344T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261201.10:c.4513-40T= ENSP00000261201.4:n.4513-40T=
ENST00000682426.1:n.2089+647T=
ENST00000682879.1:c.*3610+647T= ENSP00000508210.1:n.*3610+647T=
ENST00000683105.1:c.*536+647T= ENSP00000506801.1:n.*536+647T=
ENST00000683676.1:c.4212-6213T= ENSP00000508167.1:n.4212-6213T=
ENST00000683695.1:n.977+647T=
ENST00000684084.1:c.4461+647T= ENSP00000507859.1:n.4461+647T=
ENST00000261200.9:c.4512+647T= MANE Select ENSP00000261200.4:n.4512+647T=
ENST00000261201.9:c.4513-40T= ENSP00000261201.4:n.4513-40T=
ENST00000261200.8:c.4512+647T= ENSP00000261200.4:n.4512+647T=
ENST00000261201.8:c.4513-40T= ENSP00000261201.4:n.4513-40T=
ENST00000544039.5:c.3394-40T= ENSP00000440521.1:n.3394-40T=
NM_005691.3:c.4513-40T= NP_005682.2:n.4513-40T=
NM_020297.3:c.4512+647T= NP_064693.2:n.4512+647T=
XM_005253284.2:c.4512+647T= XP_005253341.1:n.4512+647T=
XM_005253286.2:c.4512+647T= XP_005253343.1:n.4512+647T=
XM_005253287.3:c.4513-40T= XP_005253344.1:n.4513-40T=
XM_005253288.2:c.4512+647T= XP_005253345.1:n.4512+647T=
XM_005253289.2:c.4473+647T= XP_005253346.1:n.4473+647T=
XM_005253290.2:c.4371+647T= XP_005253347.1:n.4371+647T=
XM_006719025.2:c.4474-40T= XP_006719088.1:n.4474-40T=
XM_011520545.1:c.4512+647T= XP_011518847.1:n.4512+647T=
XR_931420.1:n.632-21859A=
XR_931421.1:n.632-21859A=
XR_931422.1:n.306-21859A=
XM_005253284.4:c.4512+647T= XP_005253341.1:n.4512+647T=
XM_005253286.4:c.4512+647T= XP_005253343.1:n.4512+647T=
XM_005253287.5:c.4513-40T= XP_005253344.1:n.4513-40T=
XM_005253288.4:c.4512+647T= XP_005253345.1:n.4512+647T=
XM_005253289.4:c.4473+647T= XP_005253346.1:n.4473+647T=
XM_005253290.4:c.4371+647T= XP_005253347.1:n.4371+647T=
XM_006719025.4:c.4474-40T= XP_006719088.1:n.4474-40T=
XM_011520545.3:c.4512+647T= XP_011518847.1:n.4512+647T=
XR_931420.3:n.632-21859A=
XR_931422.2:n.318-21859A=
NM_001377273.1:c.4512+647T= NP_001364202.1:n.4512+647T=
NM_001377274.1:c.3645+647T= NP_001364203.1:n.3645+647T=
NM_005691.4:c.4513-40T= NP_005682.2:n.4513-40T=
NM_020297.4:c.4512+647T= MANE Select NP_064693.2:n.4512+647T=