Canonical Allele Identifier: CA2021314494

Gene: ABCC9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21872341_21872342delinsAG , CM000674.2:g.21872341_21872342delinsAG	GRCh38
NC_000012.11:g.22025275_22025276delinsAG , CM000674.1:g.22025275_22025276delinsAG	GRCh37
NC_000012.10:g.21916542_21916543delinsAG	NCBI36
NG_012819.1:g.69353_69354delinsCT , LRG_377:g.69353_69354delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.2198+283_2198+284delinsCT	ENSP00000261201.4:n.2198+283_2198+284delinsCT
ENST00000682068.1:c.2198+283_2198+284delinsCT	ENSP00000507226.1:n.2198+283_2198+284delinsCT
ENST00000682879.1:c.*1299+283_*1299+284delinsCT	ENSP00000508210.1:n.*1299+283_*1299+284delinsCT
ENST00000683105.1:c.2198+283_2198+284delinsCT	ENSP00000506801.1:n.2198+283_2198+284delinsCT
ENST00000683676.1:c.2198+283_2198+284delinsCT	ENSP00000508167.1:n.2198+283_2198+284delinsCT
ENST00000684084.1:c.2198+283_2198+284delinsCT	ENSP00000507859.1:n.2198+283_2198+284delinsCT
ENST00000684543.1:n.2543+283_2543+284delinsCT
ENST00000261200.9:c.2198+283_2198+284delinsCT MANE Select	ENSP00000261200.4:n.2198+283_2198+284delinsCT
ENST00000261201.9:c.2198+283_2198+284delinsCT	ENSP00000261201.4:n.2198+283_2198+284delinsCT
ENST00000261200.8:c.2198+283_2198+284delinsCT	ENSP00000261200.4:n.2198+283_2198+284delinsCT
ENST00000261201.8:c.2198+283_2198+284delinsCT	ENSP00000261201.4:n.2198+283_2198+284delinsCT
ENST00000544039.5:c.1079+283_1079+284delinsCT	ENSP00000440521.1:n.1079+283_1079+284delinsCT
NM_005691.3:c.2198+283_2198+284delinsCT	NP_005682.2:n.2198+283_2198+284delinsCT
NM_020297.3:c.2198+283_2198+284delinsCT	NP_064693.2:n.2198+283_2198+284delinsCT
XM_005253284.2:c.2198+283_2198+284delinsCT	XP_005253341.1:n.2198+283_2198+284delinsCT
XM_005253286.2:c.2198+283_2198+284delinsCT	XP_005253343.1:n.2198+283_2198+284delinsCT
XM_005253287.3:c.2198+283_2198+284delinsCT	XP_005253344.1:n.2198+283_2198+284delinsCT
XM_005253288.2:c.2198+283_2198+284delinsCT	XP_005253345.1:n.2198+283_2198+284delinsCT
XM_005253289.2:c.2198+283_2198+284delinsCT	XP_005253346.1:n.2198+283_2198+284delinsCT
XM_005253290.2:c.2198+283_2198+284delinsCT	XP_005253347.1:n.2198+283_2198+284delinsCT
XM_006719025.2:c.2198+283_2198+284delinsCT	XP_006719088.1:n.2198+283_2198+284delinsCT
XM_011520545.1:c.2198+283_2198+284delinsCT	XP_011518847.1:n.2198+283_2198+284delinsCT
XM_005253284.4:c.2198+283_2198+284delinsCT	XP_005253341.1:n.2198+283_2198+284delinsCT
XM_005253286.4:c.2198+283_2198+284delinsCT	XP_005253343.1:n.2198+283_2198+284delinsCT
XM_005253287.5:c.2198+283_2198+284delinsCT	XP_005253344.1:n.2198+283_2198+284delinsCT
XM_005253288.4:c.2198+283_2198+284delinsCT	XP_005253345.1:n.2198+283_2198+284delinsCT
XM_005253289.4:c.2198+283_2198+284delinsCT	XP_005253346.1:n.2198+283_2198+284delinsCT
XM_005253290.4:c.2198+283_2198+284delinsCT	XP_005253347.1:n.2198+283_2198+284delinsCT
XM_006719025.4:c.2198+283_2198+284delinsCT	XP_006719088.1:n.2198+283_2198+284delinsCT
XM_011520545.3:c.2198+283_2198+284delinsCT	XP_011518847.1:n.2198+283_2198+284delinsCT
NM_001377273.1:c.2198+283_2198+284delinsCT	NP_001364202.1:n.2198+283_2198+284delinsCT
NM_001377274.1:c.1334+283_1334+284delinsCT	NP_001364203.1:n.1334+283_1334+284delinsCT
NM_005691.4:c.2198+283_2198+284delinsCT	NP_005682.2:n.2198+283_2198+284delinsCT
NM_020297.4:c.2198+283_2198+284delinsCT MANE Select	NP_064693.2:n.2198+283_2198+284delinsCT