Canonical Allele Identifier: CA478870597

Gene: ABCC9

Linked Data

• MyVariant Identifiers: chr12:g.21997790A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21844856A>G , CM000674.2:g.21844856A>G	GRCh38
NC_000012.11:g.21997790A>G , CM000674.1:g.21997790A>G	GRCh37
NC_000012.10:g.21889057A>G	NCBI36
NG_012819.1:g.96839T>C , LRG_377:g.96839T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.3156T>C	ENSP00000261201.4:p.Val1052=
ENST00000682068.1:c.3156T>C	ENSP00000507226.1:p.Val1052=
ENST00000682426.1:n.733T>C
ENST00000682879.1:c.*2254T>C	ENSP00000508210.1:n.*2254T>C
ENST00000683105.1:c.3156T>C	ENSP00000506801.1:p.Val1052=
ENST00000683676.1:c.3156T>C	ENSP00000508167.1:p.Val1052=
ENST00000683811.1:n.2657T>C
ENST00000684084.1:c.3105T>C	ENSP00000507859.1:p.Val1035=
ENST00000261200.9:c.3156T>C MANE Select	ENSP00000261200.4:p.Val1052=
ENST00000261201.9:c.3156T>C	ENSP00000261201.4:p.Val1052=
ENST00000261200.8:c.3156T>C	ENSP00000261200.4:p.Val1052=
ENST00000261201.8:c.3156T>C	ENSP00000261201.4:p.Val1052=
ENST00000544039.5:c.2037T>C	ENSP00000440521.1:p.Val679=
NM_005691.3:c.3156T>C	NP_005682.2:p.Val1052=
NM_020297.3:c.3156T>C	NP_064693.2:p.Val1052=
XM_005253284.2:c.3156T>C	XP_005253341.1:p.Val1052=
XM_005253286.2:c.3156T>C	XP_005253343.1:p.Val1052=
XM_005253287.3:c.3156T>C	XP_005253344.1:p.Val1052=
XM_005253288.2:c.3156T>C	XP_005253345.1:p.Val1052=
XM_005253289.2:c.3117T>C	XP_005253346.1:p.Val1039=
XM_005253290.2:c.3015T>C	XP_005253347.1:p.Val1005=
XM_006719025.2:c.3117T>C	XP_006719088.1:p.Val1039=
XM_011520545.1:c.3156T>C	XP_011518847.1:p.Val1052=
XM_005253284.4:c.3156T>C	XP_005253341.1:p.Val1052=
XM_005253286.4:c.3156T>C	XP_005253343.1:p.Val1052=
XM_005253287.5:c.3156T>C	XP_005253344.1:p.Val1052=
XM_005253288.4:c.3156T>C	XP_005253345.1:p.Val1052=
XM_005253289.4:c.3117T>C	XP_005253346.1:p.Val1039=
XM_005253290.4:c.3015T>C	XP_005253347.1:p.Val1005=
XM_006719025.4:c.3117T>C	XP_006719088.1:p.Val1039=
XM_011520545.3:c.3156T>C	XP_011518847.1:p.Val1052=
NM_001377273.1:c.3156T>C	NP_001364202.1:p.Val1052=
NM_001377274.1:c.2289T>C	NP_001364203.1:p.Val763=
NM_005691.4:c.3156T>C	NP_005682.2:p.Val1052=
NM_020297.4:c.3156T>C MANE Select	NP_064693.2:p.Val1052=