Canonical Allele Identifier: CA2695216155

Gene: ABCC9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21845643_21845644delinsTC , CM000674.2:g.21845643_21845644delinsTC	GRCh38
NC_000012.11:g.21998577_21998578delinsTC , CM000674.1:g.21998577_21998578delinsTC	GRCh37
NC_000012.10:g.21889844_21889845delinsTC	NCBI36
NG_012819.1:g.96051_96052delinsGA , LRG_377:g.96051_96052delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000261201.10:c.3055_3056delinsGA	ENSP00000261201.4:p.Thr1019Glu
ENST00000682068.1:c.3055_3056delinsGA	ENSP00000507226.1:p.Thr1019Glu
ENST00000682426.1:n.632_633delinsGA
ENST00000682879.1:c.*2153_*2154delinsGA	ENSP00000508210.1:n.*2153_*2154delinsGA
ENST00000683105.1:c.3055_3056delinsGA	ENSP00000506801.1:p.Thr1019Glu
ENST00000683676.1:c.3055_3056delinsGA	ENSP00000508167.1:p.Thr1019Glu
ENST00000683811.1:n.2556_2557delinsGA
ENST00000684084.1:c.3004_3005delinsGA	ENSP00000507859.1:p.Thr1002Glu
ENST00000261200.9:c.3055_3056delinsGA MANE Select	ENSP00000261200.4:p.Thr1019Glu
ENST00000261201.9:c.3055_3056delinsGA	ENSP00000261201.4:p.Thr1019Glu
ENST00000261200.8:c.3055_3056delinsGA	ENSP00000261200.4:p.Thr1019Glu
ENST00000261201.8:c.3055_3056delinsGA	ENSP00000261201.4:p.Thr1019Glu
ENST00000544039.5:c.1936_1937delinsGA	ENSP00000440521.1:p.Thr646Glu
NM_005691.3:c.3055_3056delinsGA	NP_005682.2:p.Thr1019Glu
NM_020297.3:c.3055_3056delinsGA	NP_064693.2:p.Thr1019Glu
XM_005253284.2:c.3055_3056delinsGA	XP_005253341.1:p.Thr1019Glu
XM_005253286.2:c.3055_3056delinsGA	XP_005253343.1:p.Thr1019Glu
XM_005253287.3:c.3055_3056delinsGA	XP_005253344.1:p.Thr1019Glu
XM_005253288.2:c.3055_3056delinsGA	XP_005253345.1:p.Thr1019Glu
XM_005253289.2:c.3016_3017delinsGA	XP_005253346.1:p.Thr1006Glu
XM_005253290.2:c.2914_2915delinsGA	XP_005253347.1:p.Thr972Glu
XM_006719025.2:c.3016_3017delinsGA	XP_006719088.1:p.Thr1006Glu
XM_011520545.1:c.3055_3056delinsGA	XP_011518847.1:p.Thr1019Glu
XM_005253284.4:c.3055_3056delinsGA	XP_005253341.1:p.Thr1019Glu
XM_005253286.4:c.3055_3056delinsGA	XP_005253343.1:p.Thr1019Glu
XM_005253287.5:c.3055_3056delinsGA	XP_005253344.1:p.Thr1019Glu
XM_005253288.4:c.3055_3056delinsGA	XP_005253345.1:p.Thr1019Glu
XM_005253289.4:c.3016_3017delinsGA	XP_005253346.1:p.Thr1006Glu
XM_005253290.4:c.2914_2915delinsGA	XP_005253347.1:p.Thr972Glu
XM_006719025.4:c.3016_3017delinsGA	XP_006719088.1:p.Thr1006Glu
XM_011520545.3:c.3055_3056delinsGA	XP_011518847.1:p.Thr1019Glu
NM_001377273.1:c.3055_3056delinsGA	NP_001364202.1:p.Thr1019Glu
NM_001377274.1:c.2188_2189delinsGA	NP_001364203.1:p.Thr730Glu
NM_005691.4:c.3055_3056delinsGA	NP_005682.2:p.Thr1019Glu
NM_020297.4:c.3055_3056delinsGA MANE Select	NP_064693.2:p.Thr1019Glu