Canonical Allele Identifier: CA384131321

Gene: ABCC9

Linked Data

• MyVariant Identifiers: chr12:g.22086737G>A (hg19) ; chr12:g.21933803G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21933803G>A , CM000674.2:g.21933803G>A	GRCh38
NC_000012.11:g.22086737G>A , CM000674.1:g.22086737G>A	GRCh37
NC_000012.10:g.21978004G>A	NCBI36
NG_012819.1:g.7892C>T , LRG_377:g.7892C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261201.10:c.263C>T	ENSP00000261201.4:p.Ala88Val
ENST00000621589.2:c.263C>T	ENSP00000480233.1:p.Ala88Val
ENST00000682068.1:c.263C>T	ENSP00000507226.1:p.Ala88Val
ENST00000682646.1:n.519C>T
ENST00000682789.1:n.514C>T
ENST00000682879.1:c.263C>T	ENSP00000508210.1:p.Ala88Val
ENST00000683105.1:c.263C>T	ENSP00000506801.1:p.Ala88Val
ENST00000683676.1:c.263C>T	ENSP00000508167.1:p.Ala88Val
ENST00000684084.1:c.263C>T	ENSP00000507859.1:p.Ala88Val
ENST00000684435.1:c.263C>T	ENSP00000507779.1:p.Ala88Val
ENST00000684543.1:n.608C>T
ENST00000261200.9:c.263C>T MANE Select	ENSP00000261200.4:p.Ala88Val
ENST00000261201.9:c.263C>T	ENSP00000261201.4:p.Ala88Val
ENST00000636888.1:c.263C>T	ENSP00000490640.1:p.Ala88Val
ENST00000261200.8:c.263C>T	ENSP00000261200.4:p.Ala88Val
ENST00000261201.8:c.263C>T	ENSP00000261201.4:p.Ala88Val
ENST00000326684.8:c.263C>T	ENSP00000317518.4:p.Ala88Val
ENST00000538350.5:c.263C>T	ENSP00000442604.1:p.Ala88Val
ENST00000621589.1:c.263C>T	ENSP00000480233.1:p.Ala88Val
NM_005691.3:c.263C>T	NP_005682.2:p.Ala88Val
NM_020297.3:c.263C>T	NP_064693.2:p.Ala88Val
XM_005253284.2:c.263C>T	XP_005253341.1:p.Ala88Val
XM_005253286.2:c.263C>T	XP_005253343.1:p.Ala88Val
XM_005253287.3:c.263C>T	XP_005253344.1:p.Ala88Val
XM_005253288.2:c.263C>T	XP_005253345.1:p.Ala88Val
XM_005253289.2:c.263C>T	XP_005253346.1:p.Ala88Val
XM_005253290.2:c.263C>T	XP_005253347.1:p.Ala88Val
XM_006719025.2:c.263C>T	XP_006719088.1:p.Ala88Val
XM_011520545.1:c.263C>T	XP_011518847.1:p.Ala88Val
XM_005253284.4:c.263C>T	XP_005253341.1:p.Ala88Val
XM_005253286.4:c.263C>T	XP_005253343.1:p.Ala88Val
XM_005253287.5:c.263C>T	XP_005253344.1:p.Ala88Val
XM_005253288.4:c.263C>T	XP_005253345.1:p.Ala88Val
XM_005253289.4:c.263C>T	XP_005253346.1:p.Ala88Val
XM_005253290.4:c.263C>T	XP_005253347.1:p.Ala88Val
XM_006719025.4:c.263C>T	XP_006719088.1:p.Ala88Val
XM_011520545.3:c.263C>T	XP_011518847.1:p.Ala88Val
NM_001377273.1:c.263C>T	NP_001364202.1:p.Ala88Val
NM_001377274.1:c.-192C>T	NP_001364203.1:n.-192C>T
NM_005691.4:c.263C>T	NP_005682.2:p.Ala88Val
NM_020297.4:c.263C>T MANE Select	NP_064693.2:p.Ala88Val