Canonical Allele Identifier: CA2021290821

Gene: ABCC9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21805329_21805332delinsAAAG , CM000674.2:g.21805329_21805332delinsAAAG	GRCh38
NC_000012.11:g.21958263_21958266delinsAAAG , CM000674.1:g.21958263_21958266delinsAAAG	GRCh37
NC_000012.10:g.21849530_21849533delinsAAAG	NCBI36
NG_012819.1:g.136363_136366delinsCTTT , LRG_377:g.136363_136366delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.4513-21_4513-18delinsCTTT	ENSP00000261201.4:n.4513-21_4513-18delinsCTTT
ENST00000682426.1:n.2089+666_2089+669delinsCTTT
ENST00000682879.1:c.*3610+666_*3610+669delinsCTTT	ENSP00000508210.1:n.*3610+666_*3610+669delinsCTTT
ENST00000683105.1:c.*536+666_*536+669delinsCTTT	ENSP00000506801.1:n.*536+666_*536+669delinsCTTT
ENST00000683676.1:c.4212-6194_4212-6191delinsCTTT	ENSP00000508167.1:n.4212-6194_4212-6191delinsCTTT
ENST00000683695.1:n.977+666_977+669delinsCTTT
ENST00000684084.1:c.4461+666_4461+669delinsCTTT	ENSP00000507859.1:n.4461+666_4461+669delinsCTTT
ENST00000261200.9:c.4512+666_4512+669delinsCTTT MANE Select	ENSP00000261200.4:n.4512+666_4512+669delinsCTTT
ENST00000261201.9:c.4513-21_4513-18delinsCTTT	ENSP00000261201.4:n.4513-21_4513-18delinsCTTT
ENST00000261200.8:c.4512+666_4512+669delinsCTTT	ENSP00000261200.4:n.4512+666_4512+669delinsCTTT
ENST00000261201.8:c.4513-21_4513-18delinsCTTT	ENSP00000261201.4:n.4513-21_4513-18delinsCTTT
ENST00000544039.5:c.3394-21_3394-18delinsCTTT	ENSP00000440521.1:n.3394-21_3394-18delinsCTTT
NM_005691.3:c.4513-21_4513-18delinsCTTT	NP_005682.2:n.4513-21_4513-18delinsCTTT
NM_020297.3:c.4512+666_4512+669delinsCTTT	NP_064693.2:n.4512+666_4512+669delinsCTTT
XM_005253284.2:c.4512+666_4512+669delinsCTTT	XP_005253341.1:n.4512+666_4512+669delinsCTTT
XM_005253286.2:c.4512+666_4512+669delinsCTTT	XP_005253343.1:n.4512+666_4512+669delinsCTTT
XM_005253287.3:c.4513-21_4513-18delinsCTTT	XP_005253344.1:n.4513-21_4513-18delinsCTTT
XM_005253288.2:c.4512+666_4512+669delinsCTTT	XP_005253345.1:n.4512+666_4512+669delinsCTTT
XM_005253289.2:c.4473+666_4473+669delinsCTTT	XP_005253346.1:n.4473+666_4473+669delinsCTTT
XM_005253290.2:c.4371+666_4371+669delinsCTTT	XP_005253347.1:n.4371+666_4371+669delinsCTTT
XM_006719025.2:c.4474-21_4474-18delinsCTTT	XP_006719088.1:n.4474-21_4474-18delinsCTTT
XM_011520545.1:c.4512+666_4512+669delinsCTTT	XP_011518847.1:n.4512+666_4512+669delinsCTTT
XR_931420.1:n.632-21881_632-21878delinsAAAG
XR_931421.1:n.632-21881_632-21878delinsAAAG
XR_931422.1:n.306-21881_306-21878delinsAAAG
XM_005253284.4:c.4512+666_4512+669delinsCTTT	XP_005253341.1:n.4512+666_4512+669delinsCTTT
XM_005253286.4:c.4512+666_4512+669delinsCTTT	XP_005253343.1:n.4512+666_4512+669delinsCTTT
XM_005253287.5:c.4513-21_4513-18delinsCTTT	XP_005253344.1:n.4513-21_4513-18delinsCTTT
XM_005253288.4:c.4512+666_4512+669delinsCTTT	XP_005253345.1:n.4512+666_4512+669delinsCTTT
XM_005253289.4:c.4473+666_4473+669delinsCTTT	XP_005253346.1:n.4473+666_4473+669delinsCTTT
XM_005253290.4:c.4371+666_4371+669delinsCTTT	XP_005253347.1:n.4371+666_4371+669delinsCTTT
XM_006719025.4:c.4474-21_4474-18delinsCTTT	XP_006719088.1:n.4474-21_4474-18delinsCTTT
XM_011520545.3:c.4512+666_4512+669delinsCTTT	XP_011518847.1:n.4512+666_4512+669delinsCTTT
XR_931420.3:n.632-21881_632-21878delinsAAAG
XR_931422.2:n.318-21881_318-21878delinsAAAG
NM_001377273.1:c.4512+666_4512+669delinsCTTT	NP_001364202.1:n.4512+666_4512+669delinsCTTT
NM_001377274.1:c.3645+666_3645+669delinsCTTT	NP_001364203.1:n.3645+666_3645+669delinsCTTT
NM_005691.4:c.4513-21_4513-18delinsCTTT	NP_005682.2:n.4513-21_4513-18delinsCTTT
NM_020297.4:c.4512+666_4512+669delinsCTTT MANE Select	NP_064693.2:n.4512+666_4512+669delinsCTTT