Canonical Allele Identifier: CA603664294

Gene: ABCC9

Linked Data

• dbSNP Id: rs1296084392
• gnomAD v2: 12-21998070-G-GA
• gnomAD v3: 12-21845136-G-GA
• gnomAD v4: 12-21845136-G-GA
• MyVariant Identifiers: chr12:g.21998070_21998071insA (hg19) ; chr12:g.21845136_21845137insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21845136_21845137insA , CM000674.2:g.21845136_21845137insA	GRCh38
NC_000012.11:g.21998070_21998071insA , CM000674.1:g.21998070_21998071insA	GRCh37
NC_000012.10:g.21889337_21889338insA	NCBI36
NG_012819.1:g.96558_96559insT , LRG_377:g.96558_96559insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.3097-222_3097-221insT	ENSP00000261201.4:n.3097-222_3097-221insT
ENST00000682068.1:c.3097-222_3097-221insT	ENSP00000507226.1:n.3097-222_3097-221insT
ENST00000682426.1:n.674-222_674-221insT
ENST00000682879.1:c.*2195-222_*2195-221insT	ENSP00000508210.1:n.*2195-222_*2195-221insT
ENST00000683105.1:c.3097-222_3097-221insT	ENSP00000506801.1:n.3097-222_3097-221insT
ENST00000683676.1:c.3097-222_3097-221insT	ENSP00000508167.1:n.3097-222_3097-221insT
ENST00000683811.1:n.2598-222_2598-221insT
ENST00000684084.1:c.3046-222_3046-221insT	ENSP00000507859.1:n.3046-222_3046-221insT
ENST00000261200.9:c.3097-222_3097-221insT MANE Select	ENSP00000261200.4:n.3097-222_3097-221insT
ENST00000261201.9:c.3097-222_3097-221insT	ENSP00000261201.4:n.3097-222_3097-221insT
ENST00000261200.8:c.3097-222_3097-221insT	ENSP00000261200.4:n.3097-222_3097-221insT
ENST00000261201.8:c.3097-222_3097-221insT	ENSP00000261201.4:n.3097-222_3097-221insT
ENST00000544039.5:c.1978-222_1978-221insT	ENSP00000440521.1:n.1978-222_1978-221insT
NM_005691.3:c.3097-222_3097-221insT	NP_005682.2:n.3097-222_3097-221insT
NM_020297.3:c.3097-222_3097-221insT	NP_064693.2:n.3097-222_3097-221insT
XM_005253284.2:c.3097-222_3097-221insT	XP_005253341.1:n.3097-222_3097-221insT
XM_005253286.2:c.3097-222_3097-221insT	XP_005253343.1:n.3097-222_3097-221insT
XM_005253287.3:c.3097-222_3097-221insT	XP_005253344.1:n.3097-222_3097-221insT
XM_005253288.2:c.3097-222_3097-221insT	XP_005253345.1:n.3097-222_3097-221insT
XM_005253289.2:c.3058-222_3058-221insT	XP_005253346.1:n.3058-222_3058-221insT
XM_005253290.2:c.2956-222_2956-221insT	XP_005253347.1:n.2956-222_2956-221insT
XM_006719025.2:c.3058-222_3058-221insT	XP_006719088.1:n.3058-222_3058-221insT
XM_011520545.1:c.3097-222_3097-221insT	XP_011518847.1:n.3097-222_3097-221insT
XM_005253284.4:c.3097-222_3097-221insT	XP_005253341.1:n.3097-222_3097-221insT
XM_005253286.4:c.3097-222_3097-221insT	XP_005253343.1:n.3097-222_3097-221insT
XM_005253287.5:c.3097-222_3097-221insT	XP_005253344.1:n.3097-222_3097-221insT
XM_005253288.4:c.3097-222_3097-221insT	XP_005253345.1:n.3097-222_3097-221insT
XM_005253289.4:c.3058-222_3058-221insT	XP_005253346.1:n.3058-222_3058-221insT
XM_005253290.4:c.2956-222_2956-221insT	XP_005253347.1:n.2956-222_2956-221insT
XM_006719025.4:c.3058-222_3058-221insT	XP_006719088.1:n.3058-222_3058-221insT
XM_011520545.3:c.3097-222_3097-221insT	XP_011518847.1:n.3097-222_3097-221insT
NM_001377273.1:c.3097-222_3097-221insT	NP_001364202.1:n.3097-222_3097-221insT
NM_001377274.1:c.2230-222_2230-221insT	NP_001364203.1:n.2230-222_2230-221insT
NM_005691.4:c.3097-222_3097-221insT	NP_005682.2:n.3097-222_3097-221insT
NM_020297.4:c.3097-222_3097-221insT MANE Select	NP_064693.2:n.3097-222_3097-221insT