Canonical Allele Identifier: CA2021331018

Gene: ABCC9

Linked Data

• dbSNP Id: rs1948109520

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21907707_21907708insCTGAAT , CM000674.2:g.21907707_21907708insCTGAAT	GRCh38
NC_000012.11:g.22060641_22060642insCTGAAT , CM000674.1:g.22060641_22060642insCTGAAT	GRCh37
NC_000012.10:g.21951908_21951909insCTGAAT	NCBI36
NG_012819.1:g.33987_33988insATTCAG , LRG_377:g.33987_33988insATTCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.1455+369_1455+370insATTCAG	ENSP00000261201.4:n.1455+369_1455+370insATTCAG
ENST00000682068.1:c.1455+369_1455+370insATTCAG	ENSP00000507226.1:n.1455+369_1455+370insATTCAG
ENST00000682789.1:n.1706+369_1706+370insATTCAG
ENST00000682879.1:c.*556+369_*556+370insATTCAG	ENSP00000508210.1:n.*556+369_*556+370insATTCAG
ENST00000683105.1:c.1455+369_1455+370insATTCAG	ENSP00000506801.1:n.1455+369_1455+370insATTCAG
ENST00000683676.1:c.1455+369_1455+370insATTCAG	ENSP00000508167.1:n.1455+369_1455+370insATTCAG
ENST00000684084.1:c.1455+369_1455+370insATTCAG	ENSP00000507859.1:n.1455+369_1455+370insATTCAG
ENST00000684543.1:n.1800+369_1800+370insATTCAG
ENST00000261200.9:c.1455+369_1455+370insATTCAG MANE Select	ENSP00000261200.4:n.1455+369_1455+370insATTCAG
ENST00000261201.9:c.1455+369_1455+370insATTCAG	ENSP00000261201.4:n.1455+369_1455+370insATTCAG
ENST00000261200.8:c.1455+369_1455+370insATTCAG	ENSP00000261200.4:n.1455+369_1455+370insATTCAG
ENST00000261201.8:c.1455+369_1455+370insATTCAG	ENSP00000261201.4:n.1455+369_1455+370insATTCAG
ENST00000544039.5:c.444+369_444+370insATTCAG	ENSP00000440521.1:n.444+369_444+370insATTCAG
NM_005691.3:c.1455+369_1455+370insATTCAG	NP_005682.2:n.1455+369_1455+370insATTCAG
NM_020297.3:c.1455+369_1455+370insATTCAG	NP_064693.2:n.1455+369_1455+370insATTCAG
XM_005253284.2:c.1455+369_1455+370insATTCAG	XP_005253341.1:n.1455+369_1455+370insATTCAG
XM_005253286.2:c.1455+369_1455+370insATTCAG	XP_005253343.1:n.1455+369_1455+370insATTCAG
XM_005253287.3:c.1455+369_1455+370insATTCAG	XP_005253344.1:n.1455+369_1455+370insATTCAG
XM_005253288.2:c.1455+369_1455+370insATTCAG	XP_005253345.1:n.1455+369_1455+370insATTCAG
XM_005253289.2:c.1455+369_1455+370insATTCAG	XP_005253346.1:n.1455+369_1455+370insATTCAG
XM_005253290.2:c.1455+369_1455+370insATTCAG	XP_005253347.1:n.1455+369_1455+370insATTCAG
XM_006719025.2:c.1455+369_1455+370insATTCAG	XP_006719088.1:n.1455+369_1455+370insATTCAG
XM_011520545.1:c.1455+369_1455+370insATTCAG	XP_011518847.1:n.1455+369_1455+370insATTCAG
XM_005253284.4:c.1455+369_1455+370insATTCAG	XP_005253341.1:n.1455+369_1455+370insATTCAG
XM_005253286.4:c.1455+369_1455+370insATTCAG	XP_005253343.1:n.1455+369_1455+370insATTCAG
XM_005253287.5:c.1455+369_1455+370insATTCAG	XP_005253344.1:n.1455+369_1455+370insATTCAG
XM_005253288.4:c.1455+369_1455+370insATTCAG	XP_005253345.1:n.1455+369_1455+370insATTCAG
XM_005253289.4:c.1455+369_1455+370insATTCAG	XP_005253346.1:n.1455+369_1455+370insATTCAG
XM_005253290.4:c.1455+369_1455+370insATTCAG	XP_005253347.1:n.1455+369_1455+370insATTCAG
XM_006719025.4:c.1455+369_1455+370insATTCAG	XP_006719088.1:n.1455+369_1455+370insATTCAG
XM_011520545.3:c.1455+369_1455+370insATTCAG	XP_011518847.1:n.1455+369_1455+370insATTCAG
NM_001377273.1:c.1455+369_1455+370insATTCAG	NP_001364202.1:n.1455+369_1455+370insATTCAG
NM_001377274.1:c.591+369_591+370insATTCAG	NP_001364203.1:n.591+369_591+370insATTCAG
NM_005691.4:c.1455+369_1455+370insATTCAG	NP_005682.2:n.1455+369_1455+370insATTCAG
NM_020297.4:c.1455+369_1455+370insATTCAG MANE Select	NP_064693.2:n.1455+369_1455+370insATTCAG