Canonical Allele Identifier: CA603967837

Gene: ABCC9

Linked Data

• dbSNP Id: rs1592218981
• gnomAD v2: 12-22066002-T-TA
• gnomAD v3: 12-21913068-T-TA
• gnomAD v4: 12-21913068-T-TA
• MyVariant Identifiers: chr12:g.22066002_22066003insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21913068_21913069insA , CM000674.2:g.21913068_21913069insA	GRCh38
NC_000012.11:g.22066002_22066003insA , CM000674.1:g.22066002_22066003insA	GRCh37
NC_000012.10:g.21957269_21957270insA	NCBI36
NG_012819.1:g.28626_28627insT , LRG_377:g.28626_28627insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.817-3_817-2insT	ENSP00000261201.4:n.817-3_817-2insT
ENST00000682068.1:c.817-3_817-2insT	ENSP00000507226.1:n.817-3_817-2insT
ENST00000682789.1:n.1068-3_1068-2insT
ENST00000682879.1:c.407-3_407-2insT	ENSP00000508210.1:n.407-3_407-2insT
ENST00000683105.1:c.817-3_817-2insT	ENSP00000506801.1:n.817-3_817-2insT
ENST00000683676.1:c.817-3_817-2insT	ENSP00000508167.1:n.817-3_817-2insT
ENST00000684084.1:c.817-3_817-2insT	ENSP00000507859.1:n.817-3_817-2insT
ENST00000684543.1:n.1162-3_1162-2insT
ENST00000261200.9:c.817-3_817-2insT MANE Select	ENSP00000261200.4:n.817-3_817-2insT
ENST00000261201.9:c.817-3_817-2insT	ENSP00000261201.4:n.817-3_817-2insT
ENST00000261200.8:c.817-3_817-2insT	ENSP00000261200.4:n.817-3_817-2insT
ENST00000261201.8:c.817-3_817-2insT	ENSP00000261201.4:n.817-3_817-2insT
NM_005691.3:c.817-3_817-2insT	NP_005682.2:n.817-3_817-2insT
NM_020297.3:c.817-3_817-2insT	NP_064693.2:n.817-3_817-2insT
XM_005253284.2:c.817-3_817-2insT	XP_005253341.1:n.817-3_817-2insT
XM_005253286.2:c.817-3_817-2insT	XP_005253343.1:n.817-3_817-2insT
XM_005253287.3:c.817-3_817-2insT	XP_005253344.1:n.817-3_817-2insT
XM_005253288.2:c.817-3_817-2insT	XP_005253345.1:n.817-3_817-2insT
XM_005253289.2:c.817-3_817-2insT	XP_005253346.1:n.817-3_817-2insT
XM_005253290.2:c.817-3_817-2insT	XP_005253347.1:n.817-3_817-2insT
XM_006719025.2:c.817-3_817-2insT	XP_006719088.1:n.817-3_817-2insT
XM_011520545.1:c.817-3_817-2insT	XP_011518847.1:n.817-3_817-2insT
XM_005253284.4:c.817-3_817-2insT	XP_005253341.1:n.817-3_817-2insT
XM_005253286.4:c.817-3_817-2insT	XP_005253343.1:n.817-3_817-2insT
XM_005253287.5:c.817-3_817-2insT	XP_005253344.1:n.817-3_817-2insT
XM_005253288.4:c.817-3_817-2insT	XP_005253345.1:n.817-3_817-2insT
XM_005253289.4:c.817-3_817-2insT	XP_005253346.1:n.817-3_817-2insT
XM_005253290.4:c.817-3_817-2insT	XP_005253347.1:n.817-3_817-2insT
XM_006719025.4:c.817-3_817-2insT	XP_006719088.1:n.817-3_817-2insT
XM_011520545.3:c.817-3_817-2insT	XP_011518847.1:n.817-3_817-2insT
NM_001377273.1:c.817-3_817-2insT	NP_001364202.1:n.817-3_817-2insT
NM_001377274.1:c.-48-3_-48-2insT	NP_001364203.1:n.-48-3_-48-2insT
NM_005691.4:c.817-3_817-2insT	NP_005682.2:n.817-3_817-2insT
NM_020297.4:c.817-3_817-2insT MANE Select	NP_064693.2:n.817-3_817-2insT