Canonical Allele Identifier: CA2617920937

Gene: ABCC9

Linked Data

• gnomAD v4: 12-21912721-G-GAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21912721_21912722insAAA , CM000674.2:g.21912721_21912722insAAA	GRCh38
NC_000012.11:g.22065655_22065656insAAA , CM000674.1:g.22065655_22065656insAAA	GRCh37
NC_000012.10:g.21956922_21956923insAAA	NCBI36
NG_012819.1:g.28973_28974insTTT , LRG_377:g.28973_28974insTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.1011+150_1011+151insTTT	ENSP00000261201.4:n.1011+150_1011+151insTTT
ENST00000682068.1:c.1011+150_1011+151insTTT	ENSP00000507226.1:n.1011+150_1011+151insTTT
ENST00000682789.1:n.1262+150_1262+151insTTT
ENST00000682879.1:c.*112+150_*112+151insTTT	ENSP00000508210.1:n.*112+150_*112+151insTTT
ENST00000683105.1:c.1011+150_1011+151insTTT	ENSP00000506801.1:n.1011+150_1011+151insTTT
ENST00000683676.1:c.1011+150_1011+151insTTT	ENSP00000508167.1:n.1011+150_1011+151insTTT
ENST00000684084.1:c.1011+150_1011+151insTTT	ENSP00000507859.1:n.1011+150_1011+151insTTT
ENST00000684543.1:n.1356+150_1356+151insTTT
ENST00000261200.9:c.1011+150_1011+151insTTT MANE Select	ENSP00000261200.4:n.1011+150_1011+151insTTT
ENST00000261201.9:c.1011+150_1011+151insTTT	ENSP00000261201.4:n.1011+150_1011+151insTTT
ENST00000261200.8:c.1011+150_1011+151insTTT	ENSP00000261200.4:n.1011+150_1011+151insTTT
ENST00000261201.8:c.1011+150_1011+151insTTT	ENSP00000261201.4:n.1011+150_1011+151insTTT
NM_005691.3:c.1011+150_1011+151insTTT	NP_005682.2:n.1011+150_1011+151insTTT
NM_020297.3:c.1011+150_1011+151insTTT	NP_064693.2:n.1011+150_1011+151insTTT
XM_005253284.2:c.1011+150_1011+151insTTT	XP_005253341.1:n.1011+150_1011+151insTTT
XM_005253286.2:c.1011+150_1011+151insTTT	XP_005253343.1:n.1011+150_1011+151insTTT
XM_005253287.3:c.1011+150_1011+151insTTT	XP_005253344.1:n.1011+150_1011+151insTTT
XM_005253288.2:c.1011+150_1011+151insTTT	XP_005253345.1:n.1011+150_1011+151insTTT
XM_005253289.2:c.1011+150_1011+151insTTT	XP_005253346.1:n.1011+150_1011+151insTTT
XM_005253290.2:c.1011+150_1011+151insTTT	XP_005253347.1:n.1011+150_1011+151insTTT
XM_006719025.2:c.1011+150_1011+151insTTT	XP_006719088.1:n.1011+150_1011+151insTTT
XM_011520545.1:c.1011+150_1011+151insTTT	XP_011518847.1:n.1011+150_1011+151insTTT
XM_005253284.4:c.1011+150_1011+151insTTT	XP_005253341.1:n.1011+150_1011+151insTTT
XM_005253286.4:c.1011+150_1011+151insTTT	XP_005253343.1:n.1011+150_1011+151insTTT
XM_005253287.5:c.1011+150_1011+151insTTT	XP_005253344.1:n.1011+150_1011+151insTTT
XM_005253288.4:c.1011+150_1011+151insTTT	XP_005253345.1:n.1011+150_1011+151insTTT
XM_005253289.4:c.1011+150_1011+151insTTT	XP_005253346.1:n.1011+150_1011+151insTTT
XM_005253290.4:c.1011+150_1011+151insTTT	XP_005253347.1:n.1011+150_1011+151insTTT
XM_006719025.4:c.1011+150_1011+151insTTT	XP_006719088.1:n.1011+150_1011+151insTTT
XM_011520545.3:c.1011+150_1011+151insTTT	XP_011518847.1:n.1011+150_1011+151insTTT
NM_001377273.1:c.1011+150_1011+151insTTT	NP_001364202.1:n.1011+150_1011+151insTTT
NM_001377274.1:c.147+150_147+151insTTT	NP_001364203.1:n.147+150_147+151insTTT
NM_005691.4:c.1011+150_1011+151insTTT	NP_005682.2:n.1011+150_1011+151insTTT
NM_020297.4:c.1011+150_1011+151insTTT MANE Select	NP_064693.2:n.1011+150_1011+151insTTT