Canonical Allele Identifier: CA478870034

Gene: ABCC9

Linked Data

• MyVariant Identifiers: chr12:g.21997426G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21844492G>T , CM000674.2:g.21844492G>T	GRCh38
NC_000012.11:g.21997426G>T , CM000674.1:g.21997426G>T	GRCh37
NC_000012.10:g.21888693G>T	NCBI36
NG_012819.1:g.97203C>A , LRG_377:g.97203C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.3306C>A	ENSP00000261201.4:p.Ile1102=
ENST00000682068.1:c.3306C>A	ENSP00000507226.1:p.Ile1102=
ENST00000682426.1:n.883C>A
ENST00000682879.1:c.*2404C>A	ENSP00000508210.1:n.*2404C>A
ENST00000683105.1:c.3306C>A	ENSP00000506801.1:p.Ile1102=
ENST00000683676.1:c.3306C>A	ENSP00000508167.1:p.Ile1102=
ENST00000683811.1:n.2807C>A
ENST00000684084.1:c.3255C>A	ENSP00000507859.1:p.Ile1085=
ENST00000261200.9:c.3306C>A MANE Select	ENSP00000261200.4:p.Ile1102=
ENST00000261201.9:c.3306C>A	ENSP00000261201.4:p.Ile1102=
ENST00000261200.8:c.3306C>A	ENSP00000261200.4:p.Ile1102=
ENST00000261201.8:c.3306C>A	ENSP00000261201.4:p.Ile1102=
ENST00000544039.5:c.2187C>A	ENSP00000440521.1:p.Ile729=
NM_005691.3:c.3306C>A	NP_005682.2:p.Ile1102=
NM_020297.3:c.3306C>A	NP_064693.2:p.Ile1102=
XM_005253284.2:c.3306C>A	XP_005253341.1:p.Ile1102=
XM_005253286.2:c.3306C>A	XP_005253343.1:p.Ile1102=
XM_005253287.3:c.3306C>A	XP_005253344.1:p.Ile1102=
XM_005253288.2:c.3306C>A	XP_005253345.1:p.Ile1102=
XM_005253289.2:c.3267C>A	XP_005253346.1:p.Ile1089=
XM_005253290.2:c.3165C>A	XP_005253347.1:p.Ile1055=
XM_006719025.2:c.3267C>A	XP_006719088.1:p.Ile1089=
XM_011520545.1:c.3306C>A	XP_011518847.1:p.Ile1102=
XM_005253284.4:c.3306C>A	XP_005253341.1:p.Ile1102=
XM_005253286.4:c.3306C>A	XP_005253343.1:p.Ile1102=
XM_005253287.5:c.3306C>A	XP_005253344.1:p.Ile1102=
XM_005253288.4:c.3306C>A	XP_005253345.1:p.Ile1102=
XM_005253289.4:c.3267C>A	XP_005253346.1:p.Ile1089=
XM_005253290.4:c.3165C>A	XP_005253347.1:p.Ile1055=
XM_006719025.4:c.3267C>A	XP_006719088.1:p.Ile1089=
XM_011520545.3:c.3306C>A	XP_011518847.1:p.Ile1102=
NM_001377273.1:c.3306C>A	NP_001364202.1:p.Ile1102=
NM_001377274.1:c.2439C>A	NP_001364203.1:p.Ile813=
NM_005691.4:c.3306C>A	NP_005682.2:p.Ile1102=
NM_020297.4:c.3306C>A MANE Select	NP_064693.2:p.Ile1102=