Canonical Allele Identifier: CA2021308955

Gene: ABCC9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21839613_21839615delinsCAT , CM000674.2:g.21839613_21839615delinsCAT	GRCh38
NC_000012.11:g.21992547_21992549delinsCAT , CM000674.1:g.21992547_21992549delinsCAT	GRCh37
NC_000012.10:g.21883814_21883816delinsCAT	NCBI36
NG_012819.1:g.102080_102082delinsATG , LRG_377:g.102080_102082delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.3474-1445_3474-1443delinsATG	ENSP00000261201.4:n.3474-1445_3474-1443delinsATG
ENST00000682068.1:c.3474-1445_3474-1443delinsATG	ENSP00000507226.1:n.3474-1445_3474-1443delinsATG
ENST00000682426.1:n.1051-1445_1051-1443delinsATG
ENST00000682879.1:c.*2572-1445_*2572-1443delinsATG	ENSP00000508210.1:n.*2572-1445_*2572-1443delinsATG
ENST00000683105.1:c.3474-1445_3474-1443delinsATG	ENSP00000506801.1:n.3474-1445_3474-1443delinsATG
ENST00000683676.1:c.3474-1445_3474-1443delinsATG	ENSP00000508167.1:n.3474-1445_3474-1443delinsATG
ENST00000683811.1:n.2975-1445_2975-1443delinsATG
ENST00000684084.1:c.3423-1445_3423-1443delinsATG	ENSP00000507859.1:n.3423-1445_3423-1443delinsATG
ENST00000261200.9:c.3474-1445_3474-1443delinsATG MANE Select	ENSP00000261200.4:n.3474-1445_3474-1443delinsATG
ENST00000261201.9:c.3474-1445_3474-1443delinsATG	ENSP00000261201.4:n.3474-1445_3474-1443delinsATG
ENST00000261200.8:c.3474-1445_3474-1443delinsATG	ENSP00000261200.4:n.3474-1445_3474-1443delinsATG
ENST00000261201.8:c.3474-1445_3474-1443delinsATG	ENSP00000261201.4:n.3474-1445_3474-1443delinsATG
ENST00000544039.5:c.2355-1445_2355-1443delinsATG	ENSP00000440521.1:n.2355-1445_2355-1443delinsATG
NM_005691.3:c.3474-1445_3474-1443delinsATG	NP_005682.2:n.3474-1445_3474-1443delinsATG
NM_020297.3:c.3474-1445_3474-1443delinsATG	NP_064693.2:n.3474-1445_3474-1443delinsATG
XM_005253284.2:c.3474-1445_3474-1443delinsATG	XP_005253341.1:n.3474-1445_3474-1443delinsATG
XM_005253286.2:c.3474-1445_3474-1443delinsATG	XP_005253343.1:n.3474-1445_3474-1443delinsATG
XM_005253287.3:c.3474-1445_3474-1443delinsATG	XP_005253344.1:n.3474-1445_3474-1443delinsATG
XM_005253288.2:c.3474-1445_3474-1443delinsATG	XP_005253345.1:n.3474-1445_3474-1443delinsATG
XM_005253289.2:c.3435-1445_3435-1443delinsATG	XP_005253346.1:n.3435-1445_3435-1443delinsATG
XM_005253290.2:c.3333-1445_3333-1443delinsATG	XP_005253347.1:n.3333-1445_3333-1443delinsATG
XM_006719025.2:c.3435-1445_3435-1443delinsATG	XP_006719088.1:n.3435-1445_3435-1443delinsATG
XM_011520545.1:c.3474-1445_3474-1443delinsATG	XP_011518847.1:n.3474-1445_3474-1443delinsATG
XM_005253284.4:c.3474-1445_3474-1443delinsATG	XP_005253341.1:n.3474-1445_3474-1443delinsATG
XM_005253286.4:c.3474-1445_3474-1443delinsATG	XP_005253343.1:n.3474-1445_3474-1443delinsATG
XM_005253287.5:c.3474-1445_3474-1443delinsATG	XP_005253344.1:n.3474-1445_3474-1443delinsATG
XM_005253288.4:c.3474-1445_3474-1443delinsATG	XP_005253345.1:n.3474-1445_3474-1443delinsATG
XM_005253289.4:c.3435-1445_3435-1443delinsATG	XP_005253346.1:n.3435-1445_3435-1443delinsATG
XM_005253290.4:c.3333-1445_3333-1443delinsATG	XP_005253347.1:n.3333-1445_3333-1443delinsATG
XM_006719025.4:c.3435-1445_3435-1443delinsATG	XP_006719088.1:n.3435-1445_3435-1443delinsATG
XM_011520545.3:c.3474-1445_3474-1443delinsATG	XP_011518847.1:n.3474-1445_3474-1443delinsATG
NM_001377273.1:c.3474-1445_3474-1443delinsATG	NP_001364202.1:n.3474-1445_3474-1443delinsATG
NM_001377274.1:c.2607-1445_2607-1443delinsATG	NP_001364203.1:n.2607-1445_2607-1443delinsATG
NM_005691.4:c.3474-1445_3474-1443delinsATG	NP_005682.2:n.3474-1445_3474-1443delinsATG
NM_020297.4:c.3474-1445_3474-1443delinsATG MANE Select	NP_064693.2:n.3474-1445_3474-1443delinsATG