Canonical Allele Identifier: CA945532591
Gene: ABCC9 HGNC NCBI

Linked Data

dbSNP Id: rs1946150168

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21872903_21872904insT , CM000674.2:g.21872903_21872904insT GRCh38
NC_000012.11:g.22025837_22025838insT , CM000674.1:g.22025837_22025838insT GRCh37
NC_000012.10:g.21917104_21917105insT NCBI36
NG_012819.1:g.68791_68792insA , LRG_377:g.68791_68792insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261201.10:c.2093-174_2093-173insA ENSP00000261201.4:n.2093-174_2093-173insA
ENST00000682068.1:c.2093-174_2093-173insA ENSP00000507226.1:n.2093-174_2093-173insA
ENST00000682879.1:c.*1194-174_*1194-173insA ENSP00000508210.1:n.*1194-174_*1194-173insA
ENST00000683105.1:c.2093-174_2093-173insA ENSP00000506801.1:n.2093-174_2093-173insA
ENST00000683676.1:c.2093-174_2093-173insA ENSP00000508167.1:n.2093-174_2093-173insA
ENST00000684084.1:c.2093-174_2093-173insA ENSP00000507859.1:n.2093-174_2093-173insA
ENST00000684543.1:n.2438-174_2438-173insA
ENST00000261200.9:c.2093-174_2093-173insA MANE Select ENSP00000261200.4:n.2093-174_2093-173insA
ENST00000261201.9:c.2093-174_2093-173insA ENSP00000261201.4:n.2093-174_2093-173insA
ENST00000261200.8:c.2093-174_2093-173insA ENSP00000261200.4:n.2093-174_2093-173insA
ENST00000261201.8:c.2093-174_2093-173insA ENSP00000261201.4:n.2093-174_2093-173insA
ENST00000544039.5:c.974-174_974-173insA ENSP00000440521.1:n.974-174_974-173insA
NM_005691.3:c.2093-174_2093-173insA NP_005682.2:n.2093-174_2093-173insA
NM_020297.3:c.2093-174_2093-173insA NP_064693.2:n.2093-174_2093-173insA
XM_005253284.2:c.2093-174_2093-173insA XP_005253341.1:n.2093-174_2093-173insA
XM_005253286.2:c.2093-174_2093-173insA XP_005253343.1:n.2093-174_2093-173insA
XM_005253287.3:c.2093-174_2093-173insA XP_005253344.1:n.2093-174_2093-173insA
XM_005253288.2:c.2093-174_2093-173insA XP_005253345.1:n.2093-174_2093-173insA
XM_005253289.2:c.2093-174_2093-173insA XP_005253346.1:n.2093-174_2093-173insA
XM_005253290.2:c.2093-174_2093-173insA XP_005253347.1:n.2093-174_2093-173insA
XM_006719025.2:c.2093-174_2093-173insA XP_006719088.1:n.2093-174_2093-173insA
XM_011520545.1:c.2093-174_2093-173insA XP_011518847.1:n.2093-174_2093-173insA
XM_005253284.4:c.2093-174_2093-173insA XP_005253341.1:n.2093-174_2093-173insA
XM_005253286.4:c.2093-174_2093-173insA XP_005253343.1:n.2093-174_2093-173insA
XM_005253287.5:c.2093-174_2093-173insA XP_005253344.1:n.2093-174_2093-173insA
XM_005253288.4:c.2093-174_2093-173insA XP_005253345.1:n.2093-174_2093-173insA
XM_005253289.4:c.2093-174_2093-173insA XP_005253346.1:n.2093-174_2093-173insA
XM_005253290.4:c.2093-174_2093-173insA XP_005253347.1:n.2093-174_2093-173insA
XM_006719025.4:c.2093-174_2093-173insA XP_006719088.1:n.2093-174_2093-173insA
XM_011520545.3:c.2093-174_2093-173insA XP_011518847.1:n.2093-174_2093-173insA
NM_001377273.1:c.2093-174_2093-173insA NP_001364202.1:n.2093-174_2093-173insA
NM_001377274.1:c.1229-174_1229-173insA NP_001364203.1:n.1229-174_1229-173insA
NM_005691.4:c.2093-174_2093-173insA NP_005682.2:n.2093-174_2093-173insA
NM_020297.4:c.2093-174_2093-173insA MANE Select NP_064693.2:n.2093-174_2093-173insA