Canonical Allele Identifier: CA2021330506

Gene: ABCC9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21906464_21906466delinsAAG , CM000674.2:g.21906464_21906466delinsAAG	GRCh38
NC_000012.11:g.22059398_22059400delinsAAG , CM000674.1:g.22059398_22059400delinsAAG	GRCh37
NC_000012.10:g.21950665_21950667delinsAAG	NCBI36
NG_012819.1:g.35229_35231delinsCTT , LRG_377:g.35229_35231delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.1456-178_1456-176delinsCTT	ENSP00000261201.4:n.1456-178_1456-176delinsCTT
ENST00000682068.1:c.1456-178_1456-176delinsCTT	ENSP00000507226.1:n.1456-178_1456-176delinsCTT
ENST00000682789.1:n.1707-178_1707-176delinsCTT
ENST00000682879.1:c.*557-178_*557-176delinsCTT	ENSP00000508210.1:n.*557-178_*557-176delinsCTT
ENST00000683105.1:c.1456-178_1456-176delinsCTT	ENSP00000506801.1:n.1456-178_1456-176delinsCTT
ENST00000683676.1:c.1456-178_1456-176delinsCTT	ENSP00000508167.1:n.1456-178_1456-176delinsCTT
ENST00000684084.1:c.1456-178_1456-176delinsCTT	ENSP00000507859.1:n.1456-178_1456-176delinsCTT
ENST00000684543.1:n.1801-178_1801-176delinsCTT
ENST00000261200.9:c.1456-178_1456-176delinsCTT MANE Select	ENSP00000261200.4:n.1456-178_1456-176delinsCTT
ENST00000261201.9:c.1456-178_1456-176delinsCTT	ENSP00000261201.4:n.1456-178_1456-176delinsCTT
ENST00000261200.8:c.1456-178_1456-176delinsCTT	ENSP00000261200.4:n.1456-178_1456-176delinsCTT
ENST00000261201.8:c.1456-178_1456-176delinsCTT	ENSP00000261201.4:n.1456-178_1456-176delinsCTT
ENST00000544039.5:c.445-178_445-176delinsCTT	ENSP00000440521.1:n.445-178_445-176delinsCTT
NM_005691.3:c.1456-178_1456-176delinsCTT	NP_005682.2:n.1456-178_1456-176delinsCTT
NM_020297.3:c.1456-178_1456-176delinsCTT	NP_064693.2:n.1456-178_1456-176delinsCTT
XM_005253284.2:c.1456-178_1456-176delinsCTT	XP_005253341.1:n.1456-178_1456-176delinsCTT
XM_005253286.2:c.1456-178_1456-176delinsCTT	XP_005253343.1:n.1456-178_1456-176delinsCTT
XM_005253287.3:c.1456-178_1456-176delinsCTT	XP_005253344.1:n.1456-178_1456-176delinsCTT
XM_005253288.2:c.1456-178_1456-176delinsCTT	XP_005253345.1:n.1456-178_1456-176delinsCTT
XM_005253289.2:c.1456-178_1456-176delinsCTT	XP_005253346.1:n.1456-178_1456-176delinsCTT
XM_005253290.2:c.1456-178_1456-176delinsCTT	XP_005253347.1:n.1456-178_1456-176delinsCTT
XM_006719025.2:c.1456-178_1456-176delinsCTT	XP_006719088.1:n.1456-178_1456-176delinsCTT
XM_011520545.1:c.1456-178_1456-176delinsCTT	XP_011518847.1:n.1456-178_1456-176delinsCTT
XM_005253284.4:c.1456-178_1456-176delinsCTT	XP_005253341.1:n.1456-178_1456-176delinsCTT
XM_005253286.4:c.1456-178_1456-176delinsCTT	XP_005253343.1:n.1456-178_1456-176delinsCTT
XM_005253287.5:c.1456-178_1456-176delinsCTT	XP_005253344.1:n.1456-178_1456-176delinsCTT
XM_005253288.4:c.1456-178_1456-176delinsCTT	XP_005253345.1:n.1456-178_1456-176delinsCTT
XM_005253289.4:c.1456-178_1456-176delinsCTT	XP_005253346.1:n.1456-178_1456-176delinsCTT
XM_005253290.4:c.1456-178_1456-176delinsCTT	XP_005253347.1:n.1456-178_1456-176delinsCTT
XM_006719025.4:c.1456-178_1456-176delinsCTT	XP_006719088.1:n.1456-178_1456-176delinsCTT
XM_011520545.3:c.1456-178_1456-176delinsCTT	XP_011518847.1:n.1456-178_1456-176delinsCTT
NM_001377273.1:c.1456-178_1456-176delinsCTT	NP_001364202.1:n.1456-178_1456-176delinsCTT
NM_001377274.1:c.592-178_592-176delinsCTT	NP_001364203.1:n.592-178_592-176delinsCTT
NM_005691.4:c.1456-178_1456-176delinsCTT	NP_005682.2:n.1456-178_1456-176delinsCTT
NM_020297.4:c.1456-178_1456-176delinsCTT MANE Select	NP_064693.2:n.1456-178_1456-176delinsCTT