Canonical Allele Identifier: CA6480766

Gene: ABCC9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21801025A>G , CM000674.2:g.21801025A>G	GRCh38
NC_000012.11:g.21953959A>G , CM000674.1:g.21953959A>G	GRCh37
NC_000012.10:g.21845226A>G	NCBI36
NG_012819.1:g.140670T>C , LRG_377:g.140670T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_020297.4:c.*19T>C MANE Select	NP_064693.2:n.*19T>C
ENST00000261200.9:c.*19T>C MANE Select	ENSP00000261200.4:n.*19T>C
NM_001377273.1:c.*19T>C	NP_001364202.1:n.*19T>C
NM_001377274.1:c.*19T>C	NP_001364203.1:n.*19T>C
NM_005691.4:c.*195T>C	NP_005682.2:n.*195T>C
NM_020297.3:c.*19T>C	NP_064693.2:n.*19T>C
ENST00000261200.8:c.4669T>C	ENSP00000261200.4:n.4669T>C
ENST00000261201.10:c.*195T>C	ENSP00000261201.4:n.*195T>C
ENST00000261201.9:c.4845T>C	ENSP00000261201.4:n.4845T>C
ENST00000682426.1:n.2246T>C
ENST00000682879.1:c.*3767T>C	ENSP00000508210.1:n.*3767T>C
ENST00000683105.1:c.*693T>C	ENSP00000506801.1:n.*693T>C
ENST00000683676.1:c.4212-1887T>C	ENSP00000508167.1:n.4212-1887T>C
ENST00000683695.1:n.1134T>C
ENST00000684084.1:c.*19T>C	ENSP00000507859.1:n.*19T>C
XM_005253284.2:c.*19T>C	XP_005253341.1:n.*19T>C
XM_005253284.4:c.*19T>C	XP_005253341.1:n.*19T>C
XM_005253286.2:c.*19T>C	XP_005253343.1:n.*19T>C
XM_005253286.4:c.*19T>C	XP_005253343.1:n.*19T>C
XM_005253287.5:c.*195T>C	XP_005253344.1:n.*195T>C
XM_005253288.2:c.*19T>C	XP_005253345.1:n.*19T>C
XM_005253288.4:c.*19T>C	XP_005253345.1:n.*19T>C
XM_005253289.2:c.*19T>C	XP_005253346.1:n.*19T>C
XM_005253289.4:c.*19T>C	XP_005253346.1:n.*19T>C
XM_005253290.2:c.*19T>C	XP_005253347.1:n.*19T>C
XM_005253290.4:c.*19T>C	XP_005253347.1:n.*19T>C
XM_006719025.4:c.*195T>C	XP_006719088.1:n.*195T>C
XM_011520545.1:c.*19T>C	XP_011518847.1:n.*19T>C
XM_011520545.3:c.*19T>C	XP_011518847.1:n.*19T>C
XR_931420.1:n.632-26185A>G
XR_931420.3:n.632-26185A>G
XR_931421.1:n.632-26185A>G
XR_931422.1:n.306-26185A>G
XR_931422.2:n.318-26185A>G