Canonical Allele Identifier: CA29289098

Gene: DRAM2

Linked Data

• dbSNP Id: rs144808806
• gnomAD v2: 1-111663296-G-A
• gnomAD v4: 1-111120674-G-A
• MyVariant Identifiers: chr1:g.111663296G>A (hg19) ; chr1:g.111120674G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111120674G>A , CM000663.2:g.111120674G>A	GRCh38
NC_000001.10:g.111663296G>A , CM000663.1:g.111663296G>A	GRCh37
NC_000001.9:g.111464819G>A	NCBI36
NG_053089.1:g.24543C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484310.6:c.359C>T MANE Select	ENSP00000503400.1:p.Ala120Val
ENST00000539140.6:c.359C>T	ENSP00000437718.1:p.Ala120Val
ENST00000286692.8:c.359C>T	ENSP00000286692.4:p.Ala120Val
ENST00000461449.5:n.133C>T
ENST00000462092.5:n.680C>T
ENST00000480600.6:n.375C>T
ENST00000484310.5:n.603C>T
ENST00000496430.6:c.*46C>T	ENSP00000473779.1:n.*46C>T
ENST00000539140.5:c.359C>T	ENSP00000437718.1:p.Ala120Val
NM_178454.4:c.359C>T	NP_848549.3:p.Ala120Val
XM_005270469.1:c.359C>T	XP_005270526.1:p.Ala120Val
XM_005270470.1:c.359C>T	XP_005270527.1:p.Ala120Val
XM_006710361.1:c.89C>T	XP_006710424.1:p.Ala30Val
XM_006710362.1:c.89C>T	XP_006710425.1:p.Ala30Val
XM_011540707.1:c.359C>T	XP_011539009.1:p.Ala120Val
XM_011540708.1:c.359C>T	XP_011539010.1:p.Ala120Val
NM_001349881.1:c.359C>T	NP_001336810.1:p.Ala120Val
NM_001349882.1:c.359C>T	NP_001336811.1:p.Ala120Val
NM_001349884.1:c.359C>T	NP_001336813.1:p.Ala120Val
NM_001349885.1:c.359C>T	NP_001336814.1:p.Ala120Val
NM_001349886.1:c.89C>T	NP_001336815.1:p.Ala30Val
NM_001349887.1:c.89C>T	NP_001336816.1:p.Ala30Val
NM_001349888.1:c.89C>T	NP_001336817.1:p.Ala30Val
NM_001349889.1:c.-32C>T	NP_001336818.1:n.-32C>T
NM_001349890.1:c.-32C>T	NP_001336819.1:n.-32C>T
NM_001349891.1:c.-32C>T	NP_001336820.1:n.-32C>T
NM_001349892.1:c.-32C>T	NP_001336821.1:n.-32C>T
NM_001349893.1:c.-32C>T	NP_001336822.1:n.-32C>T
NM_178454.5:c.359C>T	NP_848549.3:p.Ala120Val
NR_146301.1:n.616C>T
NR_146302.1:n.476C>T
NR_146303.1:n.827C>T
NR_146304.1:n.687C>T
NR_146305.1:n.670C>T
NR_146306.1:n.642C>T
NR_146307.1:n.715C>T
NR_146308.1:n.782C>T
NM_001349881.2:c.359C>T	NP_001336810.1:p.Ala120Val
NM_001349882.2:c.359C>T	NP_001336811.1:p.Ala120Val
NM_001349884.2:c.359C>T MANE Select	NP_001336813.1:p.Ala120Val
NM_001349885.2:c.359C>T	NP_001336814.1:p.Ala120Val
NM_001349886.2:c.89C>T	NP_001336815.1:p.Ala30Val
NM_001349887.2:c.89C>T	NP_001336816.1:p.Ala30Val
NM_001349888.2:c.89C>T	NP_001336817.1:p.Ala30Val
NM_001349889.2:c.-32C>T	NP_001336818.1:n.-32C>T
NM_001349890.2:c.-32C>T	NP_001336819.1:n.-32C>T
NM_001349891.2:c.-32C>T	NP_001336820.1:n.-32C>T
NM_001349892.2:c.-32C>T	NP_001336821.1:n.-32C>T
NM_001349893.2:c.-32C>T	NP_001336822.1:n.-32C>T
NM_178454.6:c.359C>T	NP_848549.3:p.Ala120Val
NR_146301.2:n.493C>T
NR_146302.2:n.353C>T
NR_146303.2:n.704C>T
NR_146304.2:n.564C>T
NR_146305.2:n.547C>T
NR_146306.2:n.519C>T
NR_146307.2:n.592C>T
NR_146308.2:n.659C>T