Canonical Allele Identifier: CA384121705

Gene: ABCC9

Linked Data

• MyVariant Identifiers: chr12:g.22065949A>C (hg19) ; chr12:g.21913015A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21913015A>C , CM000674.2:g.21913015A>C	GRCh38
NC_000012.11:g.22065949A>C , CM000674.1:g.22065949A>C	GRCh37
NC_000012.10:g.21957216A>C	NCBI36
NG_012819.1:g.28680T>G , LRG_377:g.28680T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261201.10:c.868T>G	ENSP00000261201.4:p.Tyr290Asp
ENST00000682068.1:c.868T>G	ENSP00000507226.1:p.Tyr290Asp
ENST00000682789.1:n.1119T>G
ENST00000682879.1:c.458T>G	ENSP00000508210.1:p.Val153Gly
ENST00000683105.1:c.868T>G	ENSP00000506801.1:p.Tyr290Asp
ENST00000683676.1:c.868T>G	ENSP00000508167.1:p.Tyr290Asp
ENST00000684084.1:c.868T>G	ENSP00000507859.1:p.Tyr290Asp
ENST00000684543.1:n.1213T>G
ENST00000261200.9:c.868T>G MANE Select	ENSP00000261200.4:p.Tyr290Asp
ENST00000261201.9:c.868T>G	ENSP00000261201.4:p.Tyr290Asp
ENST00000261200.8:c.868T>G	ENSP00000261200.4:p.Tyr290Asp
ENST00000261201.8:c.868T>G	ENSP00000261201.4:p.Tyr290Asp
NM_005691.3:c.868T>G	NP_005682.2:p.Tyr290Asp
NM_020297.3:c.868T>G	NP_064693.2:p.Tyr290Asp
XM_005253284.2:c.868T>G	XP_005253341.1:p.Tyr290Asp
XM_005253286.2:c.868T>G	XP_005253343.1:p.Tyr290Asp
XM_005253287.3:c.868T>G	XP_005253344.1:p.Tyr290Asp
XM_005253288.2:c.868T>G	XP_005253345.1:p.Tyr290Asp
XM_005253289.2:c.868T>G	XP_005253346.1:p.Tyr290Asp
XM_005253290.2:c.868T>G	XP_005253347.1:p.Tyr290Asp
XM_006719025.2:c.868T>G	XP_006719088.1:p.Tyr290Asp
XM_011520545.1:c.868T>G	XP_011518847.1:p.Tyr290Asp
XM_005253284.4:c.868T>G	XP_005253341.1:p.Tyr290Asp
XM_005253286.4:c.868T>G	XP_005253343.1:p.Tyr290Asp
XM_005253287.5:c.868T>G	XP_005253344.1:p.Tyr290Asp
XM_005253288.4:c.868T>G	XP_005253345.1:p.Tyr290Asp
XM_005253289.4:c.868T>G	XP_005253346.1:p.Tyr290Asp
XM_005253290.4:c.868T>G	XP_005253347.1:p.Tyr290Asp
XM_006719025.4:c.868T>G	XP_006719088.1:p.Tyr290Asp
XM_011520545.3:c.868T>G	XP_011518847.1:p.Tyr290Asp
NM_001377273.1:c.868T>G	NP_001364202.1:p.Tyr290Asp
NM_001377274.1:c.4T>G	NP_001364203.1:p.Tyr2Asp
NM_005691.4:c.868T>G	NP_005682.2:p.Tyr290Asp
NM_020297.4:c.868T>G MANE Select	NP_064693.2:p.Tyr290Asp