Canonical Allele Identifier: CA2021290602

Gene: ABCC9

Linked Data

• dbSNP Id: rs1941753052

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21805249_21805261del , CM000674.2:g.21805249_21805261del	GRCh38
NC_000012.11:g.21958183_21958195del , CM000674.1:g.21958183_21958195del	GRCh37
NC_000012.10:g.21849450_21849462del	NCBI36
NG_012819.1:g.136435_136447del , LRG_377:g.136435_136447del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.4564_4576del	ENSP00000261201.4:p.Gly1522SerfsTer20
ENST00000682426.1:n.2089+738_2089+750del
ENST00000682879.1:c.*3610+738_*3610+750del	ENSP00000508210.1:n.*3610+738_*3610+750del
ENST00000683105.1:c.*536+738_*536+750del	ENSP00000506801.1:n.*536+738_*536+750del
ENST00000683676.1:c.4212-6122_4212-6110del	ENSP00000508167.1:n.4212-6122_4212-6110del
ENST00000683695.1:n.977+738_977+750del
ENST00000684084.1:c.4461+738_4461+750del	ENSP00000507859.1:n.4461+738_4461+750del
ENST00000261200.9:c.4512+738_4512+750del MANE Select	ENSP00000261200.4:n.4512+738_4512+750del
ENST00000261201.9:c.4564_4576del	ENSP00000261201.4:p.Gly1522SerfsTer20
ENST00000261200.8:c.4512+738_4512+750del	ENSP00000261200.4:n.4512+738_4512+750del
ENST00000261201.8:c.4564_4576del	ENSP00000261201.4:p.Gly1522SerfsTer20
ENST00000544039.5:c.3445_3457del	ENSP00000440521.1:p.Gly1149SerfsTer20
NM_005691.3:c.4564_4576del	NP_005682.2:p.Gly1522SerfsTer20
NM_020297.3:c.4512+738_4512+750del	NP_064693.2:n.4512+738_4512+750del
XM_005253284.2:c.4512+738_4512+750del	XP_005253341.1:n.4512+738_4512+750del
XM_005253286.2:c.4512+738_4512+750del	XP_005253343.1:n.4512+738_4512+750del
XM_005253287.3:c.4564_4576del	XP_005253344.1:p.Gly1522SerfsTer20
XM_005253288.2:c.4512+738_4512+750del	XP_005253345.1:n.4512+738_4512+750del
XM_005253289.2:c.4473+738_4473+750del	XP_005253346.1:n.4473+738_4473+750del
XM_005253290.2:c.4371+738_4371+750del	XP_005253347.1:n.4371+738_4371+750del
XM_006719025.2:c.4525_4537del	XP_006719088.1:p.Gly1509SerfsTer20
XM_011520545.1:c.4512+738_4512+750del	XP_011518847.1:n.4512+738_4512+750del
XR_931420.1:n.632-21961_632-21949del
XR_931421.1:n.632-21961_632-21949del
XR_931422.1:n.306-21961_306-21949del
XM_005253284.4:c.4512+738_4512+750del	XP_005253341.1:n.4512+738_4512+750del
XM_005253286.4:c.4512+738_4512+750del	XP_005253343.1:n.4512+738_4512+750del
XM_005253287.5:c.4564_4576del	XP_005253344.1:p.Gly1522SerfsTer20
XM_005253288.4:c.4512+738_4512+750del	XP_005253345.1:n.4512+738_4512+750del
XM_005253289.4:c.4473+738_4473+750del	XP_005253346.1:n.4473+738_4473+750del
XM_005253290.4:c.4371+738_4371+750del	XP_005253347.1:n.4371+738_4371+750del
XM_006719025.4:c.4525_4537del	XP_006719088.1:p.Gly1509SerfsTer20
XM_011520545.3:c.4512+738_4512+750del	XP_011518847.1:n.4512+738_4512+750del
XR_931420.3:n.632-21961_632-21949del
XR_931422.2:n.318-21961_318-21949del
NM_001377273.1:c.4512+738_4512+750del	NP_001364202.1:n.4512+738_4512+750del
NM_001377274.1:c.3645+738_3645+750del	NP_001364203.1:n.3645+738_3645+750del
NM_005691.4:c.4564_4576del	NP_005682.2:p.Gly1522SerfsTer20
NM_020297.4:c.4512+738_4512+750del MANE Select	NP_064693.2:n.4512+738_4512+750del