Canonical Allele Identifier: CA341818865

Gene: DRAM2

Linked Data

• MyVariant Identifiers: chr1:g.111663200C>T (hg19) ; chr1:g.111120578C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111120578C>T , CM000663.2:g.111120578C>T	GRCh38
NC_000001.10:g.111663200C>T , CM000663.1:g.111663200C>T	GRCh37
NC_000001.9:g.111464723C>T	NCBI36
NG_053089.1:g.24639G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484310.6:c.455G>A MANE Select	ENSP00000503400.1:p.Gly152Asp
ENST00000539140.6:c.455G>A	ENSP00000437718.1:p.Gly152Asp
ENST00000286692.8:c.455G>A	ENSP00000286692.4:p.Gly152Asp
ENST00000461449.5:n.229G>A
ENST00000462092.5:n.776G>A
ENST00000477588.5:n.19G>A
ENST00000477769.1:n.23G>A
ENST00000480600.6:n.471G>A
ENST00000484310.5:n.699G>A
ENST00000496430.6:c.*142G>A	ENSP00000473779.1:n.*142G>A
ENST00000539140.5:c.455G>A	ENSP00000437718.1:p.Gly152Asp
NM_178454.4:c.455G>A	NP_848549.3:p.Gly152Asp
XM_005270469.1:c.455G>A	XP_005270526.1:p.Gly152Asp
XM_005270470.1:c.455G>A	XP_005270527.1:p.Gly152Asp
XM_006710361.1:c.185G>A	XP_006710424.1:p.Gly62Asp
XM_006710362.1:c.185G>A	XP_006710425.1:p.Gly62Asp
XM_011540707.1:c.455G>A	XP_011539009.1:p.Gly152Asp
XM_011540708.1:c.455G>A	XP_011539010.1:p.Gly152Asp
NM_001349881.1:c.455G>A	NP_001336810.1:p.Gly152Asp
NM_001349882.1:c.455G>A	NP_001336811.1:p.Gly152Asp
NM_001349884.1:c.455G>A	NP_001336813.1:p.Gly152Asp
NM_001349885.1:c.455G>A	NP_001336814.1:p.Gly152Asp
NM_001349886.1:c.185G>A	NP_001336815.1:p.Gly62Asp
NM_001349887.1:c.185G>A	NP_001336816.1:p.Gly62Asp
NM_001349888.1:c.185G>A	NP_001336817.1:p.Gly62Asp
NM_001349889.1:c.65G>A	NP_001336818.1:p.Gly22Asp
NM_001349890.1:c.65G>A	NP_001336819.1:p.Gly22Asp
NM_001349891.1:c.65G>A	NP_001336820.1:p.Gly22Asp
NM_001349892.1:c.65G>A	NP_001336821.1:p.Gly22Asp
NM_001349893.1:c.65G>A	NP_001336822.1:p.Gly22Asp
NM_178454.5:c.455G>A	NP_848549.3:p.Gly152Asp
NR_146301.1:n.712G>A
NR_146302.1:n.572G>A
NR_146303.1:n.923G>A
NR_146304.1:n.783G>A
NR_146305.1:n.766G>A
NR_146306.1:n.738G>A
NR_146307.1:n.811G>A
NR_146308.1:n.878G>A
NM_001349881.2:c.455G>A	NP_001336810.1:p.Gly152Asp
NM_001349882.2:c.455G>A	NP_001336811.1:p.Gly152Asp
NM_001349884.2:c.455G>A MANE Select	NP_001336813.1:p.Gly152Asp
NM_001349885.2:c.455G>A	NP_001336814.1:p.Gly152Asp
NM_001349886.2:c.185G>A	NP_001336815.1:p.Gly62Asp
NM_001349887.2:c.185G>A	NP_001336816.1:p.Gly62Asp
NM_001349888.2:c.185G>A	NP_001336817.1:p.Gly62Asp
NM_001349889.2:c.65G>A	NP_001336818.1:p.Gly22Asp
NM_001349890.2:c.65G>A	NP_001336819.1:p.Gly22Asp
NM_001349891.2:c.65G>A	NP_001336820.1:p.Gly22Asp
NM_001349892.2:c.65G>A	NP_001336821.1:p.Gly22Asp
NM_001349893.2:c.65G>A	NP_001336822.1:p.Gly22Asp
NM_178454.6:c.455G>A	NP_848549.3:p.Gly152Asp
NR_146301.2:n.589G>A
NR_146302.2:n.449G>A
NR_146303.2:n.800G>A
NR_146304.2:n.660G>A
NR_146305.2:n.643G>A
NR_146306.2:n.615G>A
NR_146307.2:n.688G>A
NR_146308.2:n.755G>A