Canonical Allele Identifier: CA2739291613

Gene: ABCC9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21844839_21844848delinsG , CM000674.2:g.21844839_21844848delinsG	GRCh38
NC_000012.11:g.21997773_21997782delinsG , CM000674.1:g.21997773_21997782delinsG	GRCh37
NC_000012.10:g.21889040_21889049delinsG	NCBI36
NG_012819.1:g.96847_96856delinsC , LRG_377:g.96847_96856delinsC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.3164_3173delinsC	ENSP00000261201.4:p.Leu1055_Glu1058delinsPro
ENST00000682068.1:c.3164_3173delinsC	ENSP00000507226.1:p.Leu1055_Glu1058delinsPro
ENST00000682426.1:n.741_750delinsC
ENST00000682879.1:c.*2262_*2271delinsC	ENSP00000508210.1:n.*2262_*2271delinsC
ENST00000683105.1:c.3164_3173delinsC	ENSP00000506801.1:p.Leu1055_Glu1058delinsPro
ENST00000683676.1:c.3164_3173delinsC	ENSP00000508167.1:p.Leu1055_Glu1058delinsPro
ENST00000683811.1:n.2665_2674delinsC
ENST00000684084.1:c.3113_3122delinsC	ENSP00000507859.1:p.Leu1038_Glu1041delinsPro
ENST00000261200.9:c.3164_3173delinsC MANE Select	ENSP00000261200.4:p.Leu1055_Glu1058delinsPro
ENST00000261201.9:c.3164_3173delinsC	ENSP00000261201.4:p.Leu1055_Glu1058delinsPro
ENST00000261200.8:c.3164_3173delinsC	ENSP00000261200.4:p.Leu1055_Glu1058delinsPro
ENST00000261201.8:c.3164_3173delinsC	ENSP00000261201.4:p.Leu1055_Glu1058delinsPro
ENST00000544039.5:c.2045_2054delinsC	ENSP00000440521.1:p.Leu682_Glu685delinsPro
NM_005691.3:c.3164_3173delinsC	NP_005682.2:p.Leu1055_Glu1058delinsPro
NM_020297.3:c.3164_3173delinsC	NP_064693.2:p.Leu1055_Glu1058delinsPro
XM_005253284.2:c.3164_3173delinsC	XP_005253341.1:p.Leu1055_Glu1058delinsPro
XM_005253286.2:c.3164_3173delinsC	XP_005253343.1:p.Leu1055_Glu1058delinsPro
XM_005253287.3:c.3164_3173delinsC	XP_005253344.1:p.Leu1055_Glu1058delinsPro
XM_005253288.2:c.3164_3173delinsC	XP_005253345.1:p.Leu1055_Glu1058delinsPro
XM_005253289.2:c.3125_3134delinsC	XP_005253346.1:p.Leu1042_Glu1045delinsPro
XM_005253290.2:c.3023_3032delinsC	XP_005253347.1:p.Leu1008_Glu1011delinsPro
XM_006719025.2:c.3125_3134delinsC	XP_006719088.1:p.Leu1042_Glu1045delinsPro
XM_011520545.1:c.3164_3173delinsC	XP_011518847.1:p.Leu1055_Glu1058delinsPro
XM_005253284.4:c.3164_3173delinsC	XP_005253341.1:p.Leu1055_Glu1058delinsPro
XM_005253286.4:c.3164_3173delinsC	XP_005253343.1:p.Leu1055_Glu1058delinsPro
XM_005253287.5:c.3164_3173delinsC	XP_005253344.1:p.Leu1055_Glu1058delinsPro
XM_005253288.4:c.3164_3173delinsC	XP_005253345.1:p.Leu1055_Glu1058delinsPro
XM_005253289.4:c.3125_3134delinsC	XP_005253346.1:p.Leu1042_Glu1045delinsPro
XM_005253290.4:c.3023_3032delinsC	XP_005253347.1:p.Leu1008_Glu1011delinsPro
XM_006719025.4:c.3125_3134delinsC	XP_006719088.1:p.Leu1042_Glu1045delinsPro
XM_011520545.3:c.3164_3173delinsC	XP_011518847.1:p.Leu1055_Glu1058delinsPro
NM_001377273.1:c.3164_3173delinsC	NP_001364202.1:p.Leu1055_Glu1058delinsPro
NM_001377274.1:c.2297_2306delinsC	NP_001364203.1:p.Leu766_Glu769delinsPro
NM_005691.4:c.3164_3173delinsC	NP_005682.2:p.Leu1055_Glu1058delinsPro
NM_020297.4:c.3164_3173delinsC MANE Select	NP_064693.2:p.Leu1055_Glu1058delinsPro