Canonical Allele Identifier: CA384121621

Gene: ABCC9

Linked Data

• MyVariant Identifiers: chr12:g.22065940A>C (hg19) ; chr12:g.21913006A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21913006A>C , CM000674.2:g.21913006A>C	GRCh38
NC_000012.11:g.22065940A>C , CM000674.1:g.22065940A>C	GRCh37
NC_000012.10:g.21957207A>C	NCBI36
NG_012819.1:g.28689T>G , LRG_377:g.28689T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261201.10:c.877T>G	ENSP00000261201.4:p.Phe293Val
ENST00000682068.1:c.877T>G	ENSP00000507226.1:p.Phe293Val
ENST00000682789.1:n.1128T>G
ENST00000682879.1:c.467T>G	ENSP00000508210.1:p.Phe156Cys
ENST00000683105.1:c.877T>G	ENSP00000506801.1:p.Phe293Val
ENST00000683676.1:c.877T>G	ENSP00000508167.1:p.Phe293Val
ENST00000684084.1:c.877T>G	ENSP00000507859.1:p.Phe293Val
ENST00000684543.1:n.1222T>G
ENST00000261200.9:c.877T>G MANE Select	ENSP00000261200.4:p.Phe293Val
ENST00000261201.9:c.877T>G	ENSP00000261201.4:p.Phe293Val
ENST00000261200.8:c.877T>G	ENSP00000261200.4:p.Phe293Val
ENST00000261201.8:c.877T>G	ENSP00000261201.4:p.Phe293Val
NM_005691.3:c.877T>G	NP_005682.2:p.Phe293Val
NM_020297.3:c.877T>G	NP_064693.2:p.Phe293Val
XM_005253284.2:c.877T>G	XP_005253341.1:p.Phe293Val
XM_005253286.2:c.877T>G	XP_005253343.1:p.Phe293Val
XM_005253287.3:c.877T>G	XP_005253344.1:p.Phe293Val
XM_005253288.2:c.877T>G	XP_005253345.1:p.Phe293Val
XM_005253289.2:c.877T>G	XP_005253346.1:p.Phe293Val
XM_005253290.2:c.877T>G	XP_005253347.1:p.Phe293Val
XM_006719025.2:c.877T>G	XP_006719088.1:p.Phe293Val
XM_011520545.1:c.877T>G	XP_011518847.1:p.Phe293Val
XM_005253284.4:c.877T>G	XP_005253341.1:p.Phe293Val
XM_005253286.4:c.877T>G	XP_005253343.1:p.Phe293Val
XM_005253287.5:c.877T>G	XP_005253344.1:p.Phe293Val
XM_005253288.4:c.877T>G	XP_005253345.1:p.Phe293Val
XM_005253289.4:c.877T>G	XP_005253346.1:p.Phe293Val
XM_005253290.4:c.877T>G	XP_005253347.1:p.Phe293Val
XM_006719025.4:c.877T>G	XP_006719088.1:p.Phe293Val
XM_011520545.3:c.877T>G	XP_011518847.1:p.Phe293Val
NM_001377273.1:c.877T>G	NP_001364202.1:p.Phe293Val
NM_001377274.1:c.13T>G	NP_001364203.1:p.Phe5Val
NM_005691.4:c.877T>G	NP_005682.2:p.Phe293Val
NM_020297.4:c.877T>G MANE Select	NP_064693.2:p.Phe293Val