Canonical Allele Identifier: CA1148273326
Gene: DRAM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111120637G= , CM000663.2:g.111120637G= GRCh38
NC_000001.10:g.111663259G= , CM000663.1:g.111663259G= GRCh37
NC_000001.9:g.111464782G= NCBI36
NG_053089.1:g.24580C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000484310.6:c.396C= MANE Select ENSP00000503400.1:p.Gly132=
ENST00000539140.6:c.396C= ENSP00000437718.1:p.Gly132=
ENST00000286692.8:c.396C= ENSP00000286692.4:p.Gly132=
ENST00000461449.5:n.170C=
ENST00000462092.5:n.717C=
ENST00000480600.6:n.412C=
ENST00000484310.5:n.640C=
ENST00000496430.6:c.*83C= ENSP00000473779.1:n.*83C=
ENST00000539140.5:c.396C= ENSP00000437718.1:p.Gly132=
NM_178454.4:c.396C= NP_848549.3:p.Gly132=
XM_005270469.1:c.396C= XP_005270526.1:p.Gly132=
XM_005270470.1:c.396C= XP_005270527.1:p.Gly132=
XM_006710361.1:c.126C= XP_006710424.1:p.Gly42=
XM_006710362.1:c.126C= XP_006710425.1:p.Gly42=
XM_011540707.1:c.396C= XP_011539009.1:p.Gly132=
XM_011540708.1:c.396C= XP_011539010.1:p.Gly132=
NM_001349881.1:c.396C= NP_001336810.1:p.Gly132=
NM_001349882.1:c.396C= NP_001336811.1:p.Gly132=
NM_001349884.1:c.396C= NP_001336813.1:p.Gly132=
NM_001349885.1:c.396C= NP_001336814.1:p.Gly132=
NM_001349886.1:c.126C= NP_001336815.1:p.Gly42=
NM_001349887.1:c.126C= NP_001336816.1:p.Gly42=
NM_001349888.1:c.126C= NP_001336817.1:p.Gly42=
NM_001349889.1:c.6C= NP_001336818.1:p.Gly2=
NM_001349890.1:c.6C= NP_001336819.1:p.Gly2=
NM_001349891.1:c.6C= NP_001336820.1:p.Gly2=
NM_001349892.1:c.6C= NP_001336821.1:p.Gly2=
NM_001349893.1:c.6C= NP_001336822.1:p.Gly2=
NM_178454.5:c.396C= NP_848549.3:p.Gly132=
NR_146301.1:n.653C=
NR_146302.1:n.513C=
NR_146303.1:n.864C=
NR_146304.1:n.724C=
NR_146305.1:n.707C=
NR_146306.1:n.679C=
NR_146307.1:n.752C=
NR_146308.1:n.819C=
NM_001349881.2:c.396C= NP_001336810.1:p.Gly132=
NM_001349882.2:c.396C= NP_001336811.1:p.Gly132=
NM_001349884.2:c.396C= MANE Select NP_001336813.1:p.Gly132=
NM_001349885.2:c.396C= NP_001336814.1:p.Gly132=
NM_001349886.2:c.126C= NP_001336815.1:p.Gly42=
NM_001349887.2:c.126C= NP_001336816.1:p.Gly42=
NM_001349888.2:c.126C= NP_001336817.1:p.Gly42=
NM_001349889.2:c.6C= NP_001336818.1:p.Gly2=
NM_001349890.2:c.6C= NP_001336819.1:p.Gly2=
NM_001349891.2:c.6C= NP_001336820.1:p.Gly2=
NM_001349892.2:c.6C= NP_001336821.1:p.Gly2=
NM_001349893.2:c.6C= NP_001336822.1:p.Gly2=
NM_178454.6:c.396C= NP_848549.3:p.Gly132=
NR_146301.2:n.530C=
NR_146302.2:n.390C=
NR_146303.2:n.741C=
NR_146304.2:n.601C=
NR_146305.2:n.584C=
NR_146306.2:n.556C=
NR_146307.2:n.629C=
NR_146308.2:n.696C=