Canonical Allele Identifier: CA2617918724

Gene: ABCC9

Linked Data

• gnomAD v4: 12-21917224-G-GTAATTTCCACTATA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21917225_21917226insAATTTCCACTATAT , CM000674.2:g.21917225_21917226insAATTTCCACTATAT	GRCh38
NC_000012.11:g.22070159_22070160insAATTTCCACTATAT , CM000674.1:g.22070159_22070160insAATTTCCACTATAT	GRCh37
NC_000012.10:g.21961426_21961427insAATTTCCACTATAT	NCBI36
NG_012819.1:g.24470_24471insTATAGTGGAAATTA , LRG_377:g.24470_24471insTATAGTGGAAATTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000261201.10:c.407-122_407-121insTATAGTGGAAATTA	ENSP00000261201.4:n.407-122_407-121insTAT...
ENST00000682068.1:c.407-122_407-121insTATAGTGGAAATTA	ENSP00000507226.1:n.407-122_407-121insTAT...
ENST00000682789.1:n.658-122_658-121insTATAGTGGAAATTA
ENST00000682879.1:c.407-4159_407-4158insTATAGTGGAAATTA	ENSP00000508210.1:n.407-4159_407-4158insT...
ENST00000683105.1:c.407-122_407-121insTATAGTGGAAATTA	ENSP00000506801.1:n.407-122_407-121insTAT...
ENST00000683676.1:c.407-122_407-121insTATAGTGGAAATTA	ENSP00000508167.1:n.407-122_407-121insTAT...
ENST00000684084.1:c.407-122_407-121insTATAGTGGAAATTA	ENSP00000507859.1:n.407-122_407-121insTAT...
ENST00000684543.1:n.752-122_752-121insTATAGTGGAAATTA
ENST00000261200.9:c.407-122_407-121insTATAGTGGAAATTA MANE Select	ENSP00000261200.4:n.407-122_407-121insTAT...
ENST00000261201.9:c.407-122_407-121insTATAGTGGAAATTA	ENSP00000261201.4:n.407-122_407-121insTAT...
ENST00000261200.8:c.407-122_407-121insTATAGTGGAAATTA	ENSP00000261200.4:n.407-122_407-121insTAT...
ENST00000261201.8:c.407-122_407-121insTATAGTGGAAATTA	ENSP00000261201.4:n.407-122_407-121insTAT...
NM_005691.3:c.407-122_407-121insTATAGTGGAAATTA	NP_005682.2:n.407-122_407-121insTATAGTGGA...
NM_020297.3:c.407-122_407-121insTATAGTGGAAATTA	NP_064693.2:n.407-122_407-121insTATAGTGGA...
XM_005253284.2:c.407-122_407-121insTATAGTGGAAATTA	XP_005253341.1:n.407-122_407-121insTATAGT...
XM_005253286.2:c.407-122_407-121insTATAGTGGAAATTA	XP_005253343.1:n.407-122_407-121insTATAGT...
XM_005253287.3:c.407-122_407-121insTATAGTGGAAATTA	XP_005253344.1:n.407-122_407-121insTATAGT...
XM_005253288.2:c.407-122_407-121insTATAGTGGAAATTA	XP_005253345.1:n.407-122_407-121insTATAGT...
XM_005253289.2:c.407-122_407-121insTATAGTGGAAATTA	XP_005253346.1:n.407-122_407-121insTATAGT...
XM_005253290.2:c.407-122_407-121insTATAGTGGAAATTA	XP_005253347.1:n.407-122_407-121insTATAGT...
XM_006719025.2:c.407-122_407-121insTATAGTGGAAATTA	XP_006719088.1:n.407-122_407-121insTATAGT...
XM_011520545.1:c.407-122_407-121insTATAGTGGAAATTA	XP_011518847.1:n.407-122_407-121insTATAGT...
XM_005253284.4:c.407-122_407-121insTATAGTGGAAATTA	XP_005253341.1:n.407-122_407-121insTATAGT...
XM_005253286.4:c.407-122_407-121insTATAGTGGAAATTA	XP_005253343.1:n.407-122_407-121insTATAGT...
XM_005253287.5:c.407-122_407-121insTATAGTGGAAATTA	XP_005253344.1:n.407-122_407-121insTATAGT...
XM_005253288.4:c.407-122_407-121insTATAGTGGAAATTA	XP_005253345.1:n.407-122_407-121insTATAGT...
XM_005253289.4:c.407-122_407-121insTATAGTGGAAATTA	XP_005253346.1:n.407-122_407-121insTATAGT...
XM_005253290.4:c.407-122_407-121insTATAGTGGAAATTA	XP_005253347.1:n.407-122_407-121insTATAGT...
XM_006719025.4:c.407-122_407-121insTATAGTGGAAATTA	XP_006719088.1:n.407-122_407-121insTATAGT...
XM_011520545.3:c.407-122_407-121insTATAGTGGAAATTA	XP_011518847.1:n.407-122_407-121insTATAGT...
NM_001377273.1:c.407-122_407-121insTATAGTGGAAATTA	NP_001364202.1:n.407-122_407-121insTATAGT...
NM_001377274.1:c.-48-4159_-48-4158insTATAGTGGAAATTA	NP_001364203.1:n.-48-4159_-48-4158insTATA...
NM_005691.4:c.407-122_407-121insTATAGTGGAAATTA	NP_005682.2:n.407-122_407-121insTATAGTGGA...
NM_020297.4:c.407-122_407-121insTATAGTGGAAATTA MANE Select	NP_064693.2:n.407-122_407-121insTATAGTGGA...