Canonical Allele Identifier: CA2021314821

Gene: ABCC9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21845140_21845141delinsAA , CM000674.2:g.21845140_21845141delinsAA	GRCh38
NC_000012.11:g.21998074_21998075delinsAA , CM000674.1:g.21998074_21998075delinsAA	GRCh37
NC_000012.10:g.21889341_21889342delinsAA	NCBI36
NG_012819.1:g.96554_96555delinsTT , LRG_377:g.96554_96555delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.3097-226_3097-225delinsTT	ENSP00000261201.4:n.3097-226_3097-225delinsTT
ENST00000682068.1:c.3097-226_3097-225delinsTT	ENSP00000507226.1:n.3097-226_3097-225delinsTT
ENST00000682426.1:n.674-226_674-225delinsTT
ENST00000682879.1:c.*2195-226_*2195-225delinsTT	ENSP00000508210.1:n.*2195-226_*2195-225delinsTT
ENST00000683105.1:c.3097-226_3097-225delinsTT	ENSP00000506801.1:n.3097-226_3097-225delinsTT
ENST00000683676.1:c.3097-226_3097-225delinsTT	ENSP00000508167.1:n.3097-226_3097-225delinsTT
ENST00000683811.1:n.2598-226_2598-225delinsTT
ENST00000684084.1:c.3046-226_3046-225delinsTT	ENSP00000507859.1:n.3046-226_3046-225delinsTT
ENST00000261200.9:c.3097-226_3097-225delinsTT MANE Select	ENSP00000261200.4:n.3097-226_3097-225delinsTT
ENST00000261201.9:c.3097-226_3097-225delinsTT	ENSP00000261201.4:n.3097-226_3097-225delinsTT
ENST00000261200.8:c.3097-226_3097-225delinsTT	ENSP00000261200.4:n.3097-226_3097-225delinsTT
ENST00000261201.8:c.3097-226_3097-225delinsTT	ENSP00000261201.4:n.3097-226_3097-225delinsTT
ENST00000544039.5:c.1978-226_1978-225delinsTT	ENSP00000440521.1:n.1978-226_1978-225delinsTT
NM_005691.3:c.3097-226_3097-225delinsTT	NP_005682.2:n.3097-226_3097-225delinsTT
NM_020297.3:c.3097-226_3097-225delinsTT	NP_064693.2:n.3097-226_3097-225delinsTT
XM_005253284.2:c.3097-226_3097-225delinsTT	XP_005253341.1:n.3097-226_3097-225delinsTT
XM_005253286.2:c.3097-226_3097-225delinsTT	XP_005253343.1:n.3097-226_3097-225delinsTT
XM_005253287.3:c.3097-226_3097-225delinsTT	XP_005253344.1:n.3097-226_3097-225delinsTT
XM_005253288.2:c.3097-226_3097-225delinsTT	XP_005253345.1:n.3097-226_3097-225delinsTT
XM_005253289.2:c.3058-226_3058-225delinsTT	XP_005253346.1:n.3058-226_3058-225delinsTT
XM_005253290.2:c.2956-226_2956-225delinsTT	XP_005253347.1:n.2956-226_2956-225delinsTT
XM_006719025.2:c.3058-226_3058-225delinsTT	XP_006719088.1:n.3058-226_3058-225delinsTT
XM_011520545.1:c.3097-226_3097-225delinsTT	XP_011518847.1:n.3097-226_3097-225delinsTT
XM_005253284.4:c.3097-226_3097-225delinsTT	XP_005253341.1:n.3097-226_3097-225delinsTT
XM_005253286.4:c.3097-226_3097-225delinsTT	XP_005253343.1:n.3097-226_3097-225delinsTT
XM_005253287.5:c.3097-226_3097-225delinsTT	XP_005253344.1:n.3097-226_3097-225delinsTT
XM_005253288.4:c.3097-226_3097-225delinsTT	XP_005253345.1:n.3097-226_3097-225delinsTT
XM_005253289.4:c.3058-226_3058-225delinsTT	XP_005253346.1:n.3058-226_3058-225delinsTT
XM_005253290.4:c.2956-226_2956-225delinsTT	XP_005253347.1:n.2956-226_2956-225delinsTT
XM_006719025.4:c.3058-226_3058-225delinsTT	XP_006719088.1:n.3058-226_3058-225delinsTT
XM_011520545.3:c.3097-226_3097-225delinsTT	XP_011518847.1:n.3097-226_3097-225delinsTT
NM_001377273.1:c.3097-226_3097-225delinsTT	NP_001364202.1:n.3097-226_3097-225delinsTT
NM_001377274.1:c.2230-226_2230-225delinsTT	NP_001364203.1:n.2230-226_2230-225delinsTT
NM_005691.4:c.3097-226_3097-225delinsTT	NP_005682.2:n.3097-226_3097-225delinsTT
NM_020297.4:c.3097-226_3097-225delinsTT MANE Select	NP_064693.2:n.3097-226_3097-225delinsTT