Canonical Allele Identifier: CA2021314180

Gene: ABCC9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21844528_21844529delinsTC , CM000674.2:g.21844528_21844529delinsTC	GRCh38
NC_000012.11:g.21997462_21997463delinsTC , CM000674.1:g.21997462_21997463delinsTC	GRCh37
NC_000012.10:g.21888729_21888730delinsTC	NCBI36
NG_012819.1:g.97166_97167delinsGA , LRG_377:g.97166_97167delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.3269_3270delinsGA	ENSP00000261201.4:p.Gly1090=
ENST00000682068.1:c.3269_3270delinsGA	ENSP00000507226.1:p.Gly1090=
ENST00000682426.1:n.846_847delinsGA
ENST00000682879.1:c.*2367_*2368delinsGA	ENSP00000508210.1:n.*2367_*2368delinsGA
ENST00000683105.1:c.3269_3270delinsGA	ENSP00000506801.1:p.Gly1090=
ENST00000683676.1:c.3269_3270delinsGA	ENSP00000508167.1:p.Gly1090=
ENST00000683811.1:n.2770_2771delinsGA
ENST00000684084.1:c.3218_3219delinsGA	ENSP00000507859.1:p.Gly1073=
ENST00000261200.9:c.3269_3270delinsGA MANE Select	ENSP00000261200.4:p.Gly1090=
ENST00000261201.9:c.3269_3270delinsGA	ENSP00000261201.4:p.Gly1090=
ENST00000261200.8:c.3269_3270delinsGA	ENSP00000261200.4:p.Gly1090=
ENST00000261201.8:c.3269_3270delinsGA	ENSP00000261201.4:p.Gly1090=
ENST00000544039.5:c.2150_2151delinsGA	ENSP00000440521.1:p.Gly717=
NM_005691.3:c.3269_3270delinsGA	NP_005682.2:p.Gly1090=
NM_020297.3:c.3269_3270delinsGA	NP_064693.2:p.Gly1090=
XM_005253284.2:c.3269_3270delinsGA	XP_005253341.1:p.Gly1090=
XM_005253286.2:c.3269_3270delinsGA	XP_005253343.1:p.Gly1090=
XM_005253287.3:c.3269_3270delinsGA	XP_005253344.1:p.Gly1090=
XM_005253288.2:c.3269_3270delinsGA	XP_005253345.1:p.Gly1090=
XM_005253289.2:c.3230_3231delinsGA	XP_005253346.1:p.Gly1077=
XM_005253290.2:c.3128_3129delinsGA	XP_005253347.1:p.Gly1043=
XM_006719025.2:c.3230_3231delinsGA	XP_006719088.1:p.Gly1077=
XM_011520545.1:c.3269_3270delinsGA	XP_011518847.1:p.Gly1090=
XM_005253284.4:c.3269_3270delinsGA	XP_005253341.1:p.Gly1090=
XM_005253286.4:c.3269_3270delinsGA	XP_005253343.1:p.Gly1090=
XM_005253287.5:c.3269_3270delinsGA	XP_005253344.1:p.Gly1090=
XM_005253288.4:c.3269_3270delinsGA	XP_005253345.1:p.Gly1090=
XM_005253289.4:c.3230_3231delinsGA	XP_005253346.1:p.Gly1077=
XM_005253290.4:c.3128_3129delinsGA	XP_005253347.1:p.Gly1043=
XM_006719025.4:c.3230_3231delinsGA	XP_006719088.1:p.Gly1077=
XM_011520545.3:c.3269_3270delinsGA	XP_011518847.1:p.Gly1090=
NM_001377273.1:c.3269_3270delinsGA	NP_001364202.1:p.Gly1090=
NM_001377274.1:c.2402_2403delinsGA	NP_001364203.1:p.Gly801=
NM_005691.4:c.3269_3270delinsGA	NP_005682.2:p.Gly1090=
NM_020297.4:c.3269_3270delinsGA MANE Select	NP_064693.2:p.Gly1090=