Canonical Allele Identifier: CA2021314393

Gene: ABCC9

Linked Data

• dbSNP Id: rs1944549015

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21844683_21844685del , CM000674.2:g.21844683_21844685del	GRCh38
NC_000012.11:g.21997617_21997619del , CM000674.1:g.21997617_21997619del	GRCh37
NC_000012.10:g.21888884_21888886del	NCBI36
NG_012819.1:g.97014_97016del , LRG_377:g.97014_97016del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.3245+86_3245+88del	ENSP00000261201.4:n.3245+86_3245+88del
ENST00000682068.1:c.3245+86_3245+88del	ENSP00000507226.1:n.3245+86_3245+88del
ENST00000682426.1:n.822+86_822+88del
ENST00000682879.1:c.*2343+86_*2343+88del	ENSP00000508210.1:n.*2343+86_*2343+88del
ENST00000683105.1:c.3245+86_3245+88del	ENSP00000506801.1:n.3245+86_3245+88del
ENST00000683676.1:c.3245+86_3245+88del	ENSP00000508167.1:n.3245+86_3245+88del
ENST00000683811.1:n.2746+86_2746+88del
ENST00000684084.1:c.3194+86_3194+88del	ENSP00000507859.1:n.3194+86_3194+88del
ENST00000261200.9:c.3245+86_3245+88del MANE Select	ENSP00000261200.4:n.3245+86_3245+88del
ENST00000261201.9:c.3245+86_3245+88del	ENSP00000261201.4:n.3245+86_3245+88del
ENST00000261200.8:c.3245+86_3245+88del	ENSP00000261200.4:n.3245+86_3245+88del
ENST00000261201.8:c.3245+86_3245+88del	ENSP00000261201.4:n.3245+86_3245+88del
ENST00000544039.5:c.2126+86_2126+88del	ENSP00000440521.1:n.2126+86_2126+88del
NM_005691.3:c.3245+86_3245+88del	NP_005682.2:n.3245+86_3245+88del
NM_020297.3:c.3245+86_3245+88del	NP_064693.2:n.3245+86_3245+88del
XM_005253284.2:c.3245+86_3245+88del	XP_005253341.1:n.3245+86_3245+88del
XM_005253286.2:c.3245+86_3245+88del	XP_005253343.1:n.3245+86_3245+88del
XM_005253287.3:c.3245+86_3245+88del	XP_005253344.1:n.3245+86_3245+88del
XM_005253288.2:c.3245+86_3245+88del	XP_005253345.1:n.3245+86_3245+88del
XM_005253289.2:c.3206+86_3206+88del	XP_005253346.1:n.3206+86_3206+88del
XM_005253290.2:c.3104+86_3104+88del	XP_005253347.1:n.3104+86_3104+88del
XM_006719025.2:c.3206+86_3206+88del	XP_006719088.1:n.3206+86_3206+88del
XM_011520545.1:c.3245+86_3245+88del	XP_011518847.1:n.3245+86_3245+88del
XM_005253284.4:c.3245+86_3245+88del	XP_005253341.1:n.3245+86_3245+88del
XM_005253286.4:c.3245+86_3245+88del	XP_005253343.1:n.3245+86_3245+88del
XM_005253287.5:c.3245+86_3245+88del	XP_005253344.1:n.3245+86_3245+88del
XM_005253288.4:c.3245+86_3245+88del	XP_005253345.1:n.3245+86_3245+88del
XM_005253289.4:c.3206+86_3206+88del	XP_005253346.1:n.3206+86_3206+88del
XM_005253290.4:c.3104+86_3104+88del	XP_005253347.1:n.3104+86_3104+88del
XM_006719025.4:c.3206+86_3206+88del	XP_006719088.1:n.3206+86_3206+88del
XM_011520545.3:c.3245+86_3245+88del	XP_011518847.1:n.3245+86_3245+88del
NM_001377273.1:c.3245+86_3245+88del	NP_001364202.1:n.3245+86_3245+88del
NM_001377274.1:c.2378+86_2378+88del	NP_001364203.1:n.2378+86_2378+88del
NM_005691.4:c.3245+86_3245+88del	NP_005682.2:n.3245+86_3245+88del
NM_020297.4:c.3245+86_3245+88del MANE Select	NP_064693.2:n.3245+86_3245+88del