Canonical Allele Identifier: CA2021314837

Gene: ABCC9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21845157_21845159delinsAAG , CM000674.2:g.21845157_21845159delinsAAG	GRCh38
NC_000012.11:g.21998091_21998093delinsAAG , CM000674.1:g.21998091_21998093delinsAAG	GRCh37
NC_000012.10:g.21889358_21889360delinsAAG	NCBI36
NG_012819.1:g.96536_96538delinsCTT , LRG_377:g.96536_96538delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.3097-244_3097-242delinsCTT	ENSP00000261201.4:n.3097-244_3097-242delinsCTT
ENST00000682068.1:c.3097-244_3097-242delinsCTT	ENSP00000507226.1:n.3097-244_3097-242delinsCTT
ENST00000682426.1:n.674-244_674-242delinsCTT
ENST00000682879.1:c.*2195-244_*2195-242delinsCTT	ENSP00000508210.1:n.*2195-244_*2195-242delinsCTT
ENST00000683105.1:c.3097-244_3097-242delinsCTT	ENSP00000506801.1:n.3097-244_3097-242delinsCTT
ENST00000683676.1:c.3097-244_3097-242delinsCTT	ENSP00000508167.1:n.3097-244_3097-242delinsCTT
ENST00000683811.1:n.2598-244_2598-242delinsCTT
ENST00000684084.1:c.3046-244_3046-242delinsCTT	ENSP00000507859.1:n.3046-244_3046-242delinsCTT
ENST00000261200.9:c.3097-244_3097-242delinsCTT MANE Select	ENSP00000261200.4:n.3097-244_3097-242delinsCTT
ENST00000261201.9:c.3097-244_3097-242delinsCTT	ENSP00000261201.4:n.3097-244_3097-242delinsCTT
ENST00000261200.8:c.3097-244_3097-242delinsCTT	ENSP00000261200.4:n.3097-244_3097-242delinsCTT
ENST00000261201.8:c.3097-244_3097-242delinsCTT	ENSP00000261201.4:n.3097-244_3097-242delinsCTT
ENST00000544039.5:c.1978-244_1978-242delinsCTT	ENSP00000440521.1:n.1978-244_1978-242delinsCTT
NM_005691.3:c.3097-244_3097-242delinsCTT	NP_005682.2:n.3097-244_3097-242delinsCTT
NM_020297.3:c.3097-244_3097-242delinsCTT	NP_064693.2:n.3097-244_3097-242delinsCTT
XM_005253284.2:c.3097-244_3097-242delinsCTT	XP_005253341.1:n.3097-244_3097-242delinsCTT
XM_005253286.2:c.3097-244_3097-242delinsCTT	XP_005253343.1:n.3097-244_3097-242delinsCTT
XM_005253287.3:c.3097-244_3097-242delinsCTT	XP_005253344.1:n.3097-244_3097-242delinsCTT
XM_005253288.2:c.3097-244_3097-242delinsCTT	XP_005253345.1:n.3097-244_3097-242delinsCTT
XM_005253289.2:c.3058-244_3058-242delinsCTT	XP_005253346.1:n.3058-244_3058-242delinsCTT
XM_005253290.2:c.2956-244_2956-242delinsCTT	XP_005253347.1:n.2956-244_2956-242delinsCTT
XM_006719025.2:c.3058-244_3058-242delinsCTT	XP_006719088.1:n.3058-244_3058-242delinsCTT
XM_011520545.1:c.3097-244_3097-242delinsCTT	XP_011518847.1:n.3097-244_3097-242delinsCTT
XM_005253284.4:c.3097-244_3097-242delinsCTT	XP_005253341.1:n.3097-244_3097-242delinsCTT
XM_005253286.4:c.3097-244_3097-242delinsCTT	XP_005253343.1:n.3097-244_3097-242delinsCTT
XM_005253287.5:c.3097-244_3097-242delinsCTT	XP_005253344.1:n.3097-244_3097-242delinsCTT
XM_005253288.4:c.3097-244_3097-242delinsCTT	XP_005253345.1:n.3097-244_3097-242delinsCTT
XM_005253289.4:c.3058-244_3058-242delinsCTT	XP_005253346.1:n.3058-244_3058-242delinsCTT
XM_005253290.4:c.2956-244_2956-242delinsCTT	XP_005253347.1:n.2956-244_2956-242delinsCTT
XM_006719025.4:c.3058-244_3058-242delinsCTT	XP_006719088.1:n.3058-244_3058-242delinsCTT
XM_011520545.3:c.3097-244_3097-242delinsCTT	XP_011518847.1:n.3097-244_3097-242delinsCTT
NM_001377273.1:c.3097-244_3097-242delinsCTT	NP_001364202.1:n.3097-244_3097-242delinsCTT
NM_001377274.1:c.2230-244_2230-242delinsCTT	NP_001364203.1:n.2230-244_2230-242delinsCTT
NM_005691.4:c.3097-244_3097-242delinsCTT	NP_005682.2:n.3097-244_3097-242delinsCTT
NM_020297.4:c.3097-244_3097-242delinsCTT MANE Select	NP_064693.2:n.3097-244_3097-242delinsCTT