Canonical Allele Identifier: CA2021312813
Gene: ABCC9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21843078C= , CM000674.2:g.21843078C= GRCh38
NC_000012.11:g.21996012C= , CM000674.1:g.21996012C= GRCh37
NC_000012.10:g.21887279C= NCBI36
NG_012819.1:g.98617G= , LRG_377:g.98617G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261201.10:c.3316-607G= ENSP00000261201.4:n.3316-607G=
ENST00000682068.1:c.3316-607G= ENSP00000507226.1:n.3316-607G=
ENST00000682426.1:n.893-607G=
ENST00000682879.1:c.*2414-607G= ENSP00000508210.1:n.*2414-607G=
ENST00000683105.1:c.3316-607G= ENSP00000506801.1:n.3316-607G=
ENST00000683676.1:c.3316-607G= ENSP00000508167.1:n.3316-607G=
ENST00000683811.1:n.2817-607G=
ENST00000684084.1:c.3265-607G= ENSP00000507859.1:n.3265-607G=
ENST00000261200.9:c.3316-607G= MANE Select ENSP00000261200.4:n.3316-607G=
ENST00000261201.9:c.3316-607G= ENSP00000261201.4:n.3316-607G=
ENST00000261200.8:c.3316-607G= ENSP00000261200.4:n.3316-607G=
ENST00000261201.8:c.3316-607G= ENSP00000261201.4:n.3316-607G=
ENST00000544039.5:c.2197-607G= ENSP00000440521.1:n.2197-607G=
NM_005691.3:c.3316-607G= NP_005682.2:n.3316-607G=
NM_020297.3:c.3316-607G= NP_064693.2:n.3316-607G=
XM_005253284.2:c.3316-607G= XP_005253341.1:n.3316-607G=
XM_005253286.2:c.3316-607G= XP_005253343.1:n.3316-607G=
XM_005253287.3:c.3316-607G= XP_005253344.1:n.3316-607G=
XM_005253288.2:c.3316-607G= XP_005253345.1:n.3316-607G=
XM_005253289.2:c.3277-607G= XP_005253346.1:n.3277-607G=
XM_005253290.2:c.3175-607G= XP_005253347.1:n.3175-607G=
XM_006719025.2:c.3277-607G= XP_006719088.1:n.3277-607G=
XM_011520545.1:c.3316-607G= XP_011518847.1:n.3316-607G=
XM_005253284.4:c.3316-607G= XP_005253341.1:n.3316-607G=
XM_005253286.4:c.3316-607G= XP_005253343.1:n.3316-607G=
XM_005253287.5:c.3316-607G= XP_005253344.1:n.3316-607G=
XM_005253288.4:c.3316-607G= XP_005253345.1:n.3316-607G=
XM_005253289.4:c.3277-607G= XP_005253346.1:n.3277-607G=
XM_005253290.4:c.3175-607G= XP_005253347.1:n.3175-607G=
XM_006719025.4:c.3277-607G= XP_006719088.1:n.3277-607G=
XM_011520545.3:c.3316-607G= XP_011518847.1:n.3316-607G=
NM_001377273.1:c.3316-607G= NP_001364202.1:n.3316-607G=
NM_001377274.1:c.2449-607G= NP_001364203.1:n.2449-607G=
NM_005691.4:c.3316-607G= NP_005682.2:n.3316-607G=
NM_020297.4:c.3316-607G= MANE Select NP_064693.2:n.3316-607G=