Canonical Allele Identifier: CA2617930650

Gene: ABCC9

Linked Data

• gnomAD v4: 12-21844913-G-GTGACAATCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21844913_21844914insTGACAATCAT , CM000674.2:g.21844913_21844914insTGACAATCAT	GRCh38
NC_000012.11:g.21997847_21997848insTGACAATCAT , CM000674.1:g.21997847_21997848insTGACAATCAT	GRCh37
NC_000012.10:g.21889114_21889115insTGACAATCAT	NCBI36
NG_012819.1:g.96781_96782insATGATTGTCA , LRG_377:g.96781_96782insATGATTGTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.3098_3099insATGATTGTCA	ENSP00000261201.4:p.Tyr1034Ter
ENST00000682068.1:c.3098_3099insATGATTGTCA	ENSP00000507226.1:p.Tyr1034Ter
ENST00000682426.1:n.675_676insATGATTGTCA
ENST00000682879.1:c.*2196_*2197insATGATTGTCA	ENSP00000508210.1:n.*2196_*2197insATGATTGTCA
ENST00000683105.1:c.3098_3099insATGATTGTCA	ENSP00000506801.1:p.Tyr1034Ter
ENST00000683676.1:c.3098_3099insATGATTGTCA	ENSP00000508167.1:p.Tyr1034Ter
ENST00000683811.1:n.2599_2600insATGATTGTCA
ENST00000684084.1:c.3047_3048insATGATTGTCA	ENSP00000507859.1:p.Tyr1017Ter
ENST00000261200.9:c.3098_3099insATGATTGTCA MANE Select	ENSP00000261200.4:p.Tyr1034Ter
ENST00000261201.9:c.3098_3099insATGATTGTCA	ENSP00000261201.4:p.Tyr1034Ter
ENST00000261200.8:c.3098_3099insATGATTGTCA	ENSP00000261200.4:p.Tyr1034Ter
ENST00000261201.8:c.3098_3099insATGATTGTCA	ENSP00000261201.4:p.Tyr1034Ter
ENST00000544039.5:c.1979_1980insATGATTGTCA	ENSP00000440521.1:p.Tyr661Ter
NM_005691.3:c.3098_3099insATGATTGTCA	NP_005682.2:p.Tyr1034Ter
NM_020297.3:c.3098_3099insATGATTGTCA	NP_064693.2:p.Tyr1034Ter
XM_005253284.2:c.3098_3099insATGATTGTCA	XP_005253341.1:p.Tyr1034Ter
XM_005253286.2:c.3098_3099insATGATTGTCA	XP_005253343.1:p.Tyr1034Ter
XM_005253287.3:c.3098_3099insATGATTGTCA	XP_005253344.1:p.Tyr1034Ter
XM_005253288.2:c.3098_3099insATGATTGTCA	XP_005253345.1:p.Tyr1034Ter
XM_005253289.2:c.3059_3060insATGATTGTCA	XP_005253346.1:p.Tyr1021Ter
XM_005253290.2:c.2957_2958insATGATTGTCA	XP_005253347.1:p.Tyr987Ter
XM_006719025.2:c.3059_3060insATGATTGTCA	XP_006719088.1:p.Tyr1021Ter
XM_011520545.1:c.3098_3099insATGATTGTCA	XP_011518847.1:p.Tyr1034Ter
XM_005253284.4:c.3098_3099insATGATTGTCA	XP_005253341.1:p.Tyr1034Ter
XM_005253286.4:c.3098_3099insATGATTGTCA	XP_005253343.1:p.Tyr1034Ter
XM_005253287.5:c.3098_3099insATGATTGTCA	XP_005253344.1:p.Tyr1034Ter
XM_005253288.4:c.3098_3099insATGATTGTCA	XP_005253345.1:p.Tyr1034Ter
XM_005253289.4:c.3059_3060insATGATTGTCA	XP_005253346.1:p.Tyr1021Ter
XM_005253290.4:c.2957_2958insATGATTGTCA	XP_005253347.1:p.Tyr987Ter
XM_006719025.4:c.3059_3060insATGATTGTCA	XP_006719088.1:p.Tyr1021Ter
XM_011520545.3:c.3098_3099insATGATTGTCA	XP_011518847.1:p.Tyr1034Ter
NM_001377273.1:c.3098_3099insATGATTGTCA	NP_001364202.1:p.Tyr1034Ter
NM_001377274.1:c.2231_2232insATGATTGTCA	NP_001364203.1:p.Tyr745Ter
NM_005691.4:c.3098_3099insATGATTGTCA	NP_005682.2:p.Tyr1034Ter
NM_020297.4:c.3098_3099insATGATTGTCA MANE Select	NP_064693.2:p.Tyr1034Ter