Canonical Allele Identifier: CA2021314532

Gene: ABCC9

Linked Data

• dbSNP Id: rs1946126248

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21872412_21872413insAT , CM000674.2:g.21872412_21872413insAT	GRCh38
NC_000012.11:g.22025346_22025347insAT , CM000674.1:g.22025346_22025347insAT	GRCh37
NC_000012.10:g.21916613_21916614insAT	NCBI36
NG_012819.1:g.69282_69283insAT , LRG_377:g.69282_69283insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.2198+212_2198+213insAT	ENSP00000261201.4:n.2198+212_2198+213insAT
ENST00000682068.1:c.2198+212_2198+213insAT	ENSP00000507226.1:n.2198+212_2198+213insAT
ENST00000682879.1:c.*1299+212_*1299+213insAT	ENSP00000508210.1:n.*1299+212_*1299+213insAT
ENST00000683105.1:c.2198+212_2198+213insAT	ENSP00000506801.1:n.2198+212_2198+213insAT
ENST00000683676.1:c.2198+212_2198+213insAT	ENSP00000508167.1:n.2198+212_2198+213insAT
ENST00000684084.1:c.2198+212_2198+213insAT	ENSP00000507859.1:n.2198+212_2198+213insAT
ENST00000684543.1:n.2543+212_2543+213insAT
ENST00000261200.9:c.2198+212_2198+213insAT MANE Select	ENSP00000261200.4:n.2198+212_2198+213insAT
ENST00000261201.9:c.2198+212_2198+213insAT	ENSP00000261201.4:n.2198+212_2198+213insAT
ENST00000261200.8:c.2198+212_2198+213insAT	ENSP00000261200.4:n.2198+212_2198+213insAT
ENST00000261201.8:c.2198+212_2198+213insAT	ENSP00000261201.4:n.2198+212_2198+213insAT
ENST00000544039.5:c.1079+212_1079+213insAT	ENSP00000440521.1:n.1079+212_1079+213insAT
NM_005691.3:c.2198+212_2198+213insAT	NP_005682.2:n.2198+212_2198+213insAT
NM_020297.3:c.2198+212_2198+213insAT	NP_064693.2:n.2198+212_2198+213insAT
XM_005253284.2:c.2198+212_2198+213insAT	XP_005253341.1:n.2198+212_2198+213insAT
XM_005253286.2:c.2198+212_2198+213insAT	XP_005253343.1:n.2198+212_2198+213insAT
XM_005253287.3:c.2198+212_2198+213insAT	XP_005253344.1:n.2198+212_2198+213insAT
XM_005253288.2:c.2198+212_2198+213insAT	XP_005253345.1:n.2198+212_2198+213insAT
XM_005253289.2:c.2198+212_2198+213insAT	XP_005253346.1:n.2198+212_2198+213insAT
XM_005253290.2:c.2198+212_2198+213insAT	XP_005253347.1:n.2198+212_2198+213insAT
XM_006719025.2:c.2198+212_2198+213insAT	XP_006719088.1:n.2198+212_2198+213insAT
XM_011520545.1:c.2198+212_2198+213insAT	XP_011518847.1:n.2198+212_2198+213insAT
XM_005253284.4:c.2198+212_2198+213insAT	XP_005253341.1:n.2198+212_2198+213insAT
XM_005253286.4:c.2198+212_2198+213insAT	XP_005253343.1:n.2198+212_2198+213insAT
XM_005253287.5:c.2198+212_2198+213insAT	XP_005253344.1:n.2198+212_2198+213insAT
XM_005253288.4:c.2198+212_2198+213insAT	XP_005253345.1:n.2198+212_2198+213insAT
XM_005253289.4:c.2198+212_2198+213insAT	XP_005253346.1:n.2198+212_2198+213insAT
XM_005253290.4:c.2198+212_2198+213insAT	XP_005253347.1:n.2198+212_2198+213insAT
XM_006719025.4:c.2198+212_2198+213insAT	XP_006719088.1:n.2198+212_2198+213insAT
XM_011520545.3:c.2198+212_2198+213insAT	XP_011518847.1:n.2198+212_2198+213insAT
NM_001377273.1:c.2198+212_2198+213insAT	NP_001364202.1:n.2198+212_2198+213insAT
NM_001377274.1:c.1334+212_1334+213insAT	NP_001364203.1:n.1334+212_1334+213insAT
NM_005691.4:c.2198+212_2198+213insAT	NP_005682.2:n.2198+212_2198+213insAT
NM_020297.4:c.2198+212_2198+213insAT MANE Select	NP_064693.2:n.2198+212_2198+213insAT