Canonical Allele Identifier: CA384121688
Gene: ABCC9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21913013G>C , CM000674.2:g.21913013G>C GRCh38
NC_000012.11:g.22065947G>C , CM000674.1:g.22065947G>C GRCh37
NC_000012.10:g.21957214G>C NCBI36
NG_012819.1:g.28682C>G , LRG_377:g.28682C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261201.10:c.870C>G ENSP00000261201.4:p.Tyr290Ter
ENST00000682068.1:c.870C>G ENSP00000507226.1:p.Tyr290Ter
ENST00000682789.1:n.1121C>G
ENST00000682879.1:c.460C>G ENSP00000508210.1:p.Gln154Glu
ENST00000683105.1:c.870C>G ENSP00000506801.1:p.Tyr290Ter
ENST00000683676.1:c.870C>G ENSP00000508167.1:p.Tyr290Ter
ENST00000684084.1:c.870C>G ENSP00000507859.1:p.Tyr290Ter
ENST00000684543.1:n.1215C>G
ENST00000261200.9:c.870C>G MANE Select ENSP00000261200.4:p.Tyr290Ter
ENST00000261201.9:c.870C>G ENSP00000261201.4:p.Tyr290Ter
ENST00000261200.8:c.870C>G ENSP00000261200.4:p.Tyr290Ter
ENST00000261201.8:c.870C>G ENSP00000261201.4:p.Tyr290Ter
NM_005691.3:c.870C>G NP_005682.2:p.Tyr290Ter
NM_020297.3:c.870C>G NP_064693.2:p.Tyr290Ter
XM_005253284.2:c.870C>G XP_005253341.1:p.Tyr290Ter
XM_005253286.2:c.870C>G XP_005253343.1:p.Tyr290Ter
XM_005253287.3:c.870C>G XP_005253344.1:p.Tyr290Ter
XM_005253288.2:c.870C>G XP_005253345.1:p.Tyr290Ter
XM_005253289.2:c.870C>G XP_005253346.1:p.Tyr290Ter
XM_005253290.2:c.870C>G XP_005253347.1:p.Tyr290Ter
XM_006719025.2:c.870C>G XP_006719088.1:p.Tyr290Ter
XM_011520545.1:c.870C>G XP_011518847.1:p.Tyr290Ter
XM_005253284.4:c.870C>G XP_005253341.1:p.Tyr290Ter
XM_005253286.4:c.870C>G XP_005253343.1:p.Tyr290Ter
XM_005253287.5:c.870C>G XP_005253344.1:p.Tyr290Ter
XM_005253288.4:c.870C>G XP_005253345.1:p.Tyr290Ter
XM_005253289.4:c.870C>G XP_005253346.1:p.Tyr290Ter
XM_005253290.4:c.870C>G XP_005253347.1:p.Tyr290Ter
XM_006719025.4:c.870C>G XP_006719088.1:p.Tyr290Ter
XM_011520545.3:c.870C>G XP_011518847.1:p.Tyr290Ter
NM_001377273.1:c.870C>G NP_001364202.1:p.Tyr290Ter
NM_001377274.1:c.6C>G NP_001364203.1:p.Tyr2Ter
NM_005691.4:c.870C>G NP_005682.2:p.Tyr290Ter
NM_020297.4:c.870C>G MANE Select NP_064693.2:p.Tyr290Ter