Canonical Allele Identifier: CA2617929154

Gene: ABCC9

Linked Data

• gnomAD v4: 12-21805146-C-CGA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21805146_21805147insGA , CM000674.2:g.21805146_21805147insGA	GRCh38
NC_000012.11:g.21958080_21958081insGA , CM000674.1:g.21958080_21958081insGA	GRCh37
NC_000012.10:g.21849347_21849348insGA	NCBI36
NG_012819.1:g.136548_136549insTC , LRG_377:g.136548_136549insTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000261201.10:c.*27_*28insTC	ENSP00000261201.4:n.*27_*28insTC
ENST00000682426.1:n.2089+851_2089+852insTC
ENST00000682879.1:c.*3610+851_*3610+852insTC	ENSP00000508210.1:n.*3610+851_*3610+852insTC
ENST00000683105.1:c.*536+851_*536+852insTC	ENSP00000506801.1:n.*536+851_*536+852insTC
ENST00000683676.1:c.4212-6009_4212-6008insTC	ENSP00000508167.1:n.4212-6009_4212-6008insTC
ENST00000683695.1:n.977+851_977+852insTC
ENST00000684084.1:c.4461+851_4461+852insTC	ENSP00000507859.1:n.4461+851_4461+852insTC
ENST00000261200.9:c.4512+851_4512+852insTC MANE Select	ENSP00000261200.4:n.4512+851_4512+852insTC
ENST00000261201.9:c.4677_4678insTC	ENSP00000261201.4:n.4677_4678insTC
ENST00000261200.8:c.4512+851_4512+852insTC	ENSP00000261200.4:n.4512+851_4512+852insTC
NM_020297.3:c.4512+851_4512+852insTC	NP_064693.2:n.4512+851_4512+852insTC
XM_005253284.2:c.4512+851_4512+852insTC	XP_005253341.1:n.4512+851_4512+852insTC
XM_005253286.2:c.4512+851_4512+852insTC	XP_005253343.1:n.4512+851_4512+852insTC
XM_005253287.3:c.*27_*28insTC	XP_005253344.1:n.*27_*28insTC
XM_005253288.2:c.4512+851_4512+852insTC	XP_005253345.1:n.4512+851_4512+852insTC
XM_005253289.2:c.4473+851_4473+852insTC	XP_005253346.1:n.4473+851_4473+852insTC
XM_005253290.2:c.4371+851_4371+852insTC	XP_005253347.1:n.4371+851_4371+852insTC
XM_006719025.2:c.*27_*28insTC	XP_006719088.1:n.*27_*28insTC
XM_011520545.1:c.4512+851_4512+852insTC	XP_011518847.1:n.4512+851_4512+852insTC
XR_931420.1:n.632-22064_632-22063insGA
XR_931421.1:n.632-22064_632-22063insGA
XR_931422.1:n.306-22064_306-22063insGA
XM_005253284.4:c.4512+851_4512+852insTC	XP_005253341.1:n.4512+851_4512+852insTC
XM_005253286.4:c.4512+851_4512+852insTC	XP_005253343.1:n.4512+851_4512+852insTC
XM_005253287.5:c.*27_*28insTC	XP_005253344.1:n.*27_*28insTC
XM_005253288.4:c.4512+851_4512+852insTC	XP_005253345.1:n.4512+851_4512+852insTC
XM_005253289.4:c.4473+851_4473+852insTC	XP_005253346.1:n.4473+851_4473+852insTC
XM_005253290.4:c.4371+851_4371+852insTC	XP_005253347.1:n.4371+851_4371+852insTC
XM_006719025.4:c.*27_*28insTC	XP_006719088.1:n.*27_*28insTC
XM_011520545.3:c.4512+851_4512+852insTC	XP_011518847.1:n.4512+851_4512+852insTC
XR_931420.3:n.632-22064_632-22063insGA
XR_931422.2:n.318-22064_318-22063insGA
NM_001377273.1:c.4512+851_4512+852insTC	NP_001364202.1:n.4512+851_4512+852insTC
NM_001377274.1:c.3645+851_3645+852insTC	NP_001364203.1:n.3645+851_3645+852insTC
NM_005691.4:c.*27_*28insTC	NP_005682.2:n.*27_*28insTC
NM_020297.4:c.4512+851_4512+852insTC MANE Select	NP_064693.2:n.4512+851_4512+852insTC