Canonical Allele Identifier: CA341818887

Gene: DRAM2

Linked Data

• dbSNP Id: rs1557883636
• gnomAD v3: 1-111120587-T-G
• gnomAD v4: 1-111120587-T-G
• MyVariant Identifiers: chr1:g.111663209T>G (hg19) ; chr1:g.111120587T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111120587T>G , CM000663.2:g.111120587T>G	GRCh38
NC_000001.10:g.111663209T>G , CM000663.1:g.111663209T>G	GRCh37
NC_000001.9:g.111464732T>G	NCBI36
NG_053089.1:g.24630A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484310.6:c.446A>C MANE Select	ENSP00000503400.1:p.Lys149Thr
ENST00000539140.6:c.446A>C	ENSP00000437718.1:p.Lys149Thr
ENST00000286692.8:c.446A>C	ENSP00000286692.4:p.Lys149Thr
ENST00000461449.5:n.220A>C
ENST00000462092.5:n.767A>C
ENST00000477588.5:n.10A>C
ENST00000477769.1:n.14A>C
ENST00000480600.6:n.462A>C
ENST00000484310.5:n.690A>C
ENST00000496430.6:c.*133A>C	ENSP00000473779.1:n.*133A>C
ENST00000539140.5:c.446A>C	ENSP00000437718.1:p.Lys149Thr
NM_178454.4:c.446A>C	NP_848549.3:p.Lys149Thr
XM_005270469.1:c.446A>C	XP_005270526.1:p.Lys149Thr
XM_005270470.1:c.446A>C	XP_005270527.1:p.Lys149Thr
XM_006710361.1:c.176A>C	XP_006710424.1:p.Lys59Thr
XM_006710362.1:c.176A>C	XP_006710425.1:p.Lys59Thr
XM_011540707.1:c.446A>C	XP_011539009.1:p.Lys149Thr
XM_011540708.1:c.446A>C	XP_011539010.1:p.Lys149Thr
NM_001349881.1:c.446A>C	NP_001336810.1:p.Lys149Thr
NM_001349882.1:c.446A>C	NP_001336811.1:p.Lys149Thr
NM_001349884.1:c.446A>C	NP_001336813.1:p.Lys149Thr
NM_001349885.1:c.446A>C	NP_001336814.1:p.Lys149Thr
NM_001349886.1:c.176A>C	NP_001336815.1:p.Lys59Thr
NM_001349887.1:c.176A>C	NP_001336816.1:p.Lys59Thr
NM_001349888.1:c.176A>C	NP_001336817.1:p.Lys59Thr
NM_001349889.1:c.56A>C	NP_001336818.1:p.Lys19Thr
NM_001349890.1:c.56A>C	NP_001336819.1:p.Lys19Thr
NM_001349891.1:c.56A>C	NP_001336820.1:p.Lys19Thr
NM_001349892.1:c.56A>C	NP_001336821.1:p.Lys19Thr
NM_001349893.1:c.56A>C	NP_001336822.1:p.Lys19Thr
NM_178454.5:c.446A>C	NP_848549.3:p.Lys149Thr
NR_146301.1:n.703A>C
NR_146302.1:n.563A>C
NR_146303.1:n.914A>C
NR_146304.1:n.774A>C
NR_146305.1:n.757A>C
NR_146306.1:n.729A>C
NR_146307.1:n.802A>C
NR_146308.1:n.869A>C
NM_001349881.2:c.446A>C	NP_001336810.1:p.Lys149Thr
NM_001349882.2:c.446A>C	NP_001336811.1:p.Lys149Thr
NM_001349884.2:c.446A>C MANE Select	NP_001336813.1:p.Lys149Thr
NM_001349885.2:c.446A>C	NP_001336814.1:p.Lys149Thr
NM_001349886.2:c.176A>C	NP_001336815.1:p.Lys59Thr
NM_001349887.2:c.176A>C	NP_001336816.1:p.Lys59Thr
NM_001349888.2:c.176A>C	NP_001336817.1:p.Lys59Thr
NM_001349889.2:c.56A>C	NP_001336818.1:p.Lys19Thr
NM_001349890.2:c.56A>C	NP_001336819.1:p.Lys19Thr
NM_001349891.2:c.56A>C	NP_001336820.1:p.Lys19Thr
NM_001349892.2:c.56A>C	NP_001336821.1:p.Lys19Thr
NM_001349893.2:c.56A>C	NP_001336822.1:p.Lys19Thr
NM_178454.6:c.446A>C	NP_848549.3:p.Lys149Thr
NR_146301.2:n.580A>C
NR_146302.2:n.440A>C
NR_146303.2:n.791A>C
NR_146304.2:n.651A>C
NR_146305.2:n.634A>C
NR_146306.2:n.606A>C
NR_146307.2:n.679A>C
NR_146308.2:n.746A>C