Canonical Allele Identifier: CA384124558

Gene: ABCC9

Linked Data

• MyVariant Identifiers: chr12:g.22005309G>T (hg19) ; chr12:g.21852375G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21852375G>T , CM000674.2:g.21852375G>T	GRCh38
NC_000012.11:g.22005309G>T , CM000674.1:g.22005309G>T	GRCh37
NC_000012.10:g.21896576G>T	NCBI36
NG_012819.1:g.89320C>A , LRG_377:g.89320C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.2636C>A	ENSP00000261201.4:p.Ala879Asp
ENST00000682068.1:c.2636C>A	ENSP00000507226.1:p.Ala879Asp
ENST00000682426.1:n.213C>A
ENST00000682879.1:c.*1734C>A	ENSP00000508210.1:n.*1734C>A
ENST00000683105.1:c.2636C>A	ENSP00000506801.1:p.Ala879Asp
ENST00000683676.1:c.2636C>A	ENSP00000508167.1:p.Ala879Asp
ENST00000683811.1:n.2137C>A
ENST00000684084.1:c.2585C>A	ENSP00000507859.1:p.Ala862Asp
ENST00000261200.9:c.2636C>A MANE Select	ENSP00000261200.4:p.Ala879Asp
ENST00000261201.9:c.2636C>A	ENSP00000261201.4:p.Ala879Asp
ENST00000261200.8:c.2636C>A	ENSP00000261200.4:p.Ala879Asp
ENST00000261201.8:c.2636C>A	ENSP00000261201.4:p.Ala879Asp
ENST00000544039.5:c.1517C>A	ENSP00000440521.1:p.Ala506Asp
NM_005691.3:c.2636C>A	NP_005682.2:p.Ala879Asp
NM_020297.3:c.2636C>A	NP_064693.2:p.Ala879Asp
XM_005253284.2:c.2636C>A	XP_005253341.1:p.Ala879Asp
XM_005253286.2:c.2636C>A	XP_005253343.1:p.Ala879Asp
XM_005253287.3:c.2636C>A	XP_005253344.1:p.Ala879Asp
XM_005253288.2:c.2636C>A	XP_005253345.1:p.Ala879Asp
XM_005253289.2:c.2597C>A	XP_005253346.1:p.Ala866Asp
XM_005253290.2:c.2495C>A	XP_005253347.1:p.Ala832Asp
XM_006719025.2:c.2597C>A	XP_006719088.1:p.Ala866Asp
XM_011520545.1:c.2636C>A	XP_011518847.1:p.Ala879Asp
XM_005253284.4:c.2636C>A	XP_005253341.1:p.Ala879Asp
XM_005253286.4:c.2636C>A	XP_005253343.1:p.Ala879Asp
XM_005253287.5:c.2636C>A	XP_005253344.1:p.Ala879Asp
XM_005253288.4:c.2636C>A	XP_005253345.1:p.Ala879Asp
XM_005253289.4:c.2597C>A	XP_005253346.1:p.Ala866Asp
XM_005253290.4:c.2495C>A	XP_005253347.1:p.Ala832Asp
XM_006719025.4:c.2597C>A	XP_006719088.1:p.Ala866Asp
XM_011520545.3:c.2636C>A	XP_011518847.1:p.Ala879Asp
NM_001377273.1:c.2636C>A	NP_001364202.1:p.Ala879Asp
NM_001377274.1:c.1769C>A	NP_001364203.1:p.Ala590Asp
NM_005691.4:c.2636C>A	NP_005682.2:p.Ala879Asp
NM_020297.4:c.2636C>A MANE Select	NP_064693.2:p.Ala879Asp