Canonical Allele Identifier: CA2021330466

Gene: ABCC9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21906362_21906363delinsAG , CM000674.2:g.21906362_21906363delinsAG	GRCh38
NC_000012.11:g.22059296_22059297delinsAG , CM000674.1:g.22059296_22059297delinsAG	GRCh37
NC_000012.10:g.21950563_21950564delinsAG	NCBI36
NG_012819.1:g.35332_35333delinsCT , LRG_377:g.35332_35333delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.1456-75_1456-74delinsCT	ENSP00000261201.4:n.1456-75_1456-74delinsCT
ENST00000682068.1:c.1456-75_1456-74delinsCT	ENSP00000507226.1:n.1456-75_1456-74delinsCT
ENST00000682789.1:n.1707-75_1707-74delinsCT
ENST00000682879.1:c.*557-75_*557-74delinsCT	ENSP00000508210.1:n.*557-75_*557-74delinsCT
ENST00000683105.1:c.1456-75_1456-74delinsCT	ENSP00000506801.1:n.1456-75_1456-74delinsCT
ENST00000683676.1:c.1456-75_1456-74delinsCT	ENSP00000508167.1:n.1456-75_1456-74delinsCT
ENST00000684084.1:c.1456-75_1456-74delinsCT	ENSP00000507859.1:n.1456-75_1456-74delinsCT
ENST00000684543.1:n.1801-75_1801-74delinsCT
ENST00000261200.9:c.1456-75_1456-74delinsCT MANE Select	ENSP00000261200.4:n.1456-75_1456-74delinsCT
ENST00000261201.9:c.1456-75_1456-74delinsCT	ENSP00000261201.4:n.1456-75_1456-74delinsCT
ENST00000261200.8:c.1456-75_1456-74delinsCT	ENSP00000261200.4:n.1456-75_1456-74delinsCT
ENST00000261201.8:c.1456-75_1456-74delinsCT	ENSP00000261201.4:n.1456-75_1456-74delinsCT
ENST00000544039.5:c.445-75_445-74delinsCT	ENSP00000440521.1:n.445-75_445-74delinsCT
NM_005691.3:c.1456-75_1456-74delinsCT	NP_005682.2:n.1456-75_1456-74delinsCT
NM_020297.3:c.1456-75_1456-74delinsCT	NP_064693.2:n.1456-75_1456-74delinsCT
XM_005253284.2:c.1456-75_1456-74delinsCT	XP_005253341.1:n.1456-75_1456-74delinsCT
XM_005253286.2:c.1456-75_1456-74delinsCT	XP_005253343.1:n.1456-75_1456-74delinsCT
XM_005253287.3:c.1456-75_1456-74delinsCT	XP_005253344.1:n.1456-75_1456-74delinsCT
XM_005253288.2:c.1456-75_1456-74delinsCT	XP_005253345.1:n.1456-75_1456-74delinsCT
XM_005253289.2:c.1456-75_1456-74delinsCT	XP_005253346.1:n.1456-75_1456-74delinsCT
XM_005253290.2:c.1456-75_1456-74delinsCT	XP_005253347.1:n.1456-75_1456-74delinsCT
XM_006719025.2:c.1456-75_1456-74delinsCT	XP_006719088.1:n.1456-75_1456-74delinsCT
XM_011520545.1:c.1456-75_1456-74delinsCT	XP_011518847.1:n.1456-75_1456-74delinsCT
XM_005253284.4:c.1456-75_1456-74delinsCT	XP_005253341.1:n.1456-75_1456-74delinsCT
XM_005253286.4:c.1456-75_1456-74delinsCT	XP_005253343.1:n.1456-75_1456-74delinsCT
XM_005253287.5:c.1456-75_1456-74delinsCT	XP_005253344.1:n.1456-75_1456-74delinsCT
XM_005253288.4:c.1456-75_1456-74delinsCT	XP_005253345.1:n.1456-75_1456-74delinsCT
XM_005253289.4:c.1456-75_1456-74delinsCT	XP_005253346.1:n.1456-75_1456-74delinsCT
XM_005253290.4:c.1456-75_1456-74delinsCT	XP_005253347.1:n.1456-75_1456-74delinsCT
XM_006719025.4:c.1456-75_1456-74delinsCT	XP_006719088.1:n.1456-75_1456-74delinsCT
XM_011520545.3:c.1456-75_1456-74delinsCT	XP_011518847.1:n.1456-75_1456-74delinsCT
NM_001377273.1:c.1456-75_1456-74delinsCT	NP_001364202.1:n.1456-75_1456-74delinsCT
NM_001377274.1:c.592-75_592-74delinsCT	NP_001364203.1:n.592-75_592-74delinsCT
NM_005691.4:c.1456-75_1456-74delinsCT	NP_005682.2:n.1456-75_1456-74delinsCT
NM_020297.4:c.1456-75_1456-74delinsCT MANE Select	NP_064693.2:n.1456-75_1456-74delinsCT