Canonical Allele Identifier: CA6480767

Gene: ABCC9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21801037C>T , CM000674.2:g.21801037C>T	GRCh38
NC_000012.11:g.21953971C>T , CM000674.1:g.21953971C>T	GRCh37
NC_000012.10:g.21845238C>T	NCBI36
NG_012819.1:g.140658G>A , LRG_377:g.140658G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.*183G>A	ENSP00000261201.4:n.*183G>A
ENST00000682426.1:n.2234G>A
ENST00000682879.1:c.*3755G>A	ENSP00000508210.1:n.*3755G>A
ENST00000683105.1:c.*681G>A	ENSP00000506801.1:n.*681G>A
ENST00000683676.1:c.4212-1899G>A	ENSP00000508167.1:n.4212-1899G>A
ENST00000683695.1:n.1122G>A
ENST00000684084.1:c.*7G>A	ENSP00000507859.1:n.*7G>A
ENST00000261200.9:c.*7G>A MANE Select	ENSP00000261200.4:n.*7G>A
ENST00000261201.9:c.4833G>A	ENSP00000261201.4:n.4833G>A
ENST00000261200.8:c.4657G>A	ENSP00000261200.4:n.4657G>A
NM_020297.3:c.*7G>A	NP_064693.2:n.*7G>A
XM_005253284.2:c.*7G>A	XP_005253341.1:n.*7G>A
XM_005253286.2:c.*7G>A	XP_005253343.1:n.*7G>A
XM_005253288.2:c.*7G>A	XP_005253345.1:n.*7G>A
XM_005253289.2:c.*7G>A	XP_005253346.1:n.*7G>A
XM_005253290.2:c.*7G>A	XP_005253347.1:n.*7G>A
XM_011520545.1:c.*7G>A	XP_011518847.1:n.*7G>A
XR_931420.1:n.632-26173C>T
XR_931421.1:n.632-26173C>T
XR_931422.1:n.306-26173C>T
XM_005253284.4:c.*7G>A	XP_005253341.1:n.*7G>A
XM_005253286.4:c.*7G>A	XP_005253343.1:n.*7G>A
XM_005253287.5:c.*183G>A	XP_005253344.1:n.*183G>A
XM_005253288.4:c.*7G>A	XP_005253345.1:n.*7G>A
XM_005253289.4:c.*7G>A	XP_005253346.1:n.*7G>A
XM_005253290.4:c.*7G>A	XP_005253347.1:n.*7G>A
XM_006719025.4:c.*183G>A	XP_006719088.1:n.*183G>A
XM_011520545.3:c.*7G>A	XP_011518847.1:n.*7G>A
XR_931420.3:n.632-26173C>T
XR_931422.2:n.318-26173C>T
NM_001377273.1:c.*7G>A	NP_001364202.1:n.*7G>A
NM_001377274.1:c.*7G>A	NP_001364203.1:n.*7G>A
NM_005691.4:c.*183G>A	NP_005682.2:n.*183G>A
NM_020297.4:c.*7G>A MANE Select	NP_064693.2:n.*7G>A