Canonical Allele Identifier: CA1188789444

Gene: DRAM2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111120683_111120684delinsAG , CM000663.2:g.111120683_111120684delinsAG	GRCh38
NC_000001.10:g.111663305_111663306delinsAG , CM000663.1:g.111663305_111663306delinsAG	GRCh37
NC_000001.9:g.111464828_111464829delinsAG	NCBI36
NG_053089.1:g.24533_24534delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484310.6:c.349_350delinsCT MANE Select	ENSP00000503400.1:p.Leu117=
ENST00000539140.6:c.349_350delinsCT	ENSP00000437718.1:p.Leu117=
ENST00000286692.8:c.349_350delinsCT	ENSP00000286692.4:p.Leu117=
ENST00000461449.5:n.123_124delinsCT
ENST00000462092.5:n.670_671delinsCT
ENST00000480600.6:n.365_366delinsCT
ENST00000484310.5:n.593_594delinsCT
ENST00000496430.6:c.*36_*37delinsCT	ENSP00000473779.1:n.*36_*37delinsCT
ENST00000539140.5:c.349_350delinsCT	ENSP00000437718.1:p.Leu117=
NM_178454.4:c.349_350delinsCT	NP_848549.3:p.Leu117=
XM_005270469.1:c.349_350delinsCT	XP_005270526.1:p.Leu117=
XM_005270470.1:c.349_350delinsCT	XP_005270527.1:p.Leu117=
XM_006710361.1:c.79_80delinsCT	XP_006710424.1:p.Leu27=
XM_006710362.1:c.79_80delinsCT	XP_006710425.1:p.Leu27=
XM_011540707.1:c.349_350delinsCT	XP_011539009.1:p.Leu117=
XM_011540708.1:c.349_350delinsCT	XP_011539010.1:p.Leu117=
NM_001349881.1:c.349_350delinsCT	NP_001336810.1:p.Leu117=
NM_001349882.1:c.349_350delinsCT	NP_001336811.1:p.Leu117=
NM_001349884.1:c.349_350delinsCT	NP_001336813.1:p.Leu117=
NM_001349885.1:c.349_350delinsCT	NP_001336814.1:p.Leu117=
NM_001349886.1:c.79_80delinsCT	NP_001336815.1:p.Leu27=
NM_001349887.1:c.79_80delinsCT	NP_001336816.1:p.Leu27=
NM_001349888.1:c.79_80delinsCT	NP_001336817.1:p.Leu27=
NM_001349889.1:c.-42_-41delinsCT	NP_001336818.1:n.-42_-41delinsCT
NM_001349890.1:c.-42_-41delinsCT	NP_001336819.1:n.-42_-41delinsCT
NM_001349891.1:c.-42_-41delinsCT	NP_001336820.1:n.-42_-41delinsCT
NM_001349892.1:c.-42_-41delinsCT	NP_001336821.1:n.-42_-41delinsCT
NM_001349893.1:c.-42_-41delinsCT	NP_001336822.1:n.-42_-41delinsCT
NM_178454.5:c.349_350delinsCT	NP_848549.3:p.Leu117=
NR_146301.1:n.606_607delinsCT
NR_146302.1:n.466_467delinsCT
NR_146303.1:n.817_818delinsCT
NR_146304.1:n.677_678delinsCT
NR_146305.1:n.660_661delinsCT
NR_146306.1:n.632_633delinsCT
NR_146307.1:n.705_706delinsCT
NR_146308.1:n.772_773delinsCT
NM_001349881.2:c.349_350delinsCT	NP_001336810.1:p.Leu117=
NM_001349882.2:c.349_350delinsCT	NP_001336811.1:p.Leu117=
NM_001349884.2:c.349_350delinsCT MANE Select	NP_001336813.1:p.Leu117=
NM_001349885.2:c.349_350delinsCT	NP_001336814.1:p.Leu117=
NM_001349886.2:c.79_80delinsCT	NP_001336815.1:p.Leu27=
NM_001349887.2:c.79_80delinsCT	NP_001336816.1:p.Leu27=
NM_001349888.2:c.79_80delinsCT	NP_001336817.1:p.Leu27=
NM_001349889.2:c.-42_-41delinsCT	NP_001336818.1:n.-42_-41delinsCT
NM_001349890.2:c.-42_-41delinsCT	NP_001336819.1:n.-42_-41delinsCT
NM_001349891.2:c.-42_-41delinsCT	NP_001336820.1:n.-42_-41delinsCT
NM_001349892.2:c.-42_-41delinsCT	NP_001336821.1:n.-42_-41delinsCT
NM_001349893.2:c.-42_-41delinsCT	NP_001336822.1:n.-42_-41delinsCT
NM_178454.6:c.349_350delinsCT	NP_848549.3:p.Leu117=
NR_146301.2:n.483_484delinsCT
NR_146302.2:n.343_344delinsCT
NR_146303.2:n.694_695delinsCT
NR_146304.2:n.554_555delinsCT
NR_146305.2:n.537_538delinsCT
NR_146306.2:n.509_510delinsCT
NR_146307.2:n.582_583delinsCT
NR_146308.2:n.649_650delinsCT