Canonical Allele Identifier: CA341819027

Gene: DRAM2

Linked Data

• MyVariant Identifiers: chr1:g.111663270A>T (hg19) ; chr1:g.111120648A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111120648A>T , CM000663.2:g.111120648A>T	GRCh38
NC_000001.10:g.111663270A>T , CM000663.1:g.111663270A>T	GRCh37
NC_000001.9:g.111464793A>T	NCBI36
NG_053089.1:g.24569T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484310.6:c.385T>A MANE Select	ENSP00000503400.1:p.Phe129Ile
ENST00000539140.6:c.385T>A	ENSP00000437718.1:p.Phe129Ile
ENST00000286692.8:c.385T>A	ENSP00000286692.4:p.Phe129Ile
ENST00000461449.5:n.159T>A
ENST00000462092.5:n.706T>A
ENST00000480600.6:n.401T>A
ENST00000484310.5:n.629T>A
ENST00000496430.6:c.*72T>A	ENSP00000473779.1:n.*72T>A
ENST00000539140.5:c.385T>A	ENSP00000437718.1:p.Phe129Ile
NM_178454.4:c.385T>A	NP_848549.3:p.Phe129Ile
XM_005270469.1:c.385T>A	XP_005270526.1:p.Phe129Ile
XM_005270470.1:c.385T>A	XP_005270527.1:p.Phe129Ile
XM_006710361.1:c.115T>A	XP_006710424.1:p.Phe39Ile
XM_006710362.1:c.115T>A	XP_006710425.1:p.Phe39Ile
XM_011540707.1:c.385T>A	XP_011539009.1:p.Phe129Ile
XM_011540708.1:c.385T>A	XP_011539010.1:p.Phe129Ile
NM_001349881.1:c.385T>A	NP_001336810.1:p.Phe129Ile
NM_001349882.1:c.385T>A	NP_001336811.1:p.Phe129Ile
NM_001349884.1:c.385T>A	NP_001336813.1:p.Phe129Ile
NM_001349885.1:c.385T>A	NP_001336814.1:p.Phe129Ile
NM_001349886.1:c.115T>A	NP_001336815.1:p.Phe39Ile
NM_001349887.1:c.115T>A	NP_001336816.1:p.Phe39Ile
NM_001349888.1:c.115T>A	NP_001336817.1:p.Phe39Ile
NM_001349889.1:c.-6T>A	NP_001336818.1:n.-6T>A
NM_001349890.1:c.-6T>A	NP_001336819.1:n.-6T>A
NM_001349891.1:c.-6T>A	NP_001336820.1:n.-6T>A
NM_001349892.1:c.-6T>A	NP_001336821.1:n.-6T>A
NM_001349893.1:c.-6T>A	NP_001336822.1:n.-6T>A
NM_178454.5:c.385T>A	NP_848549.3:p.Phe129Ile
NR_146301.1:n.642T>A
NR_146302.1:n.502T>A
NR_146303.1:n.853T>A
NR_146304.1:n.713T>A
NR_146305.1:n.696T>A
NR_146306.1:n.668T>A
NR_146307.1:n.741T>A
NR_146308.1:n.808T>A
NM_001349881.2:c.385T>A	NP_001336810.1:p.Phe129Ile
NM_001349882.2:c.385T>A	NP_001336811.1:p.Phe129Ile
NM_001349884.2:c.385T>A MANE Select	NP_001336813.1:p.Phe129Ile
NM_001349885.2:c.385T>A	NP_001336814.1:p.Phe129Ile
NM_001349886.2:c.115T>A	NP_001336815.1:p.Phe39Ile
NM_001349887.2:c.115T>A	NP_001336816.1:p.Phe39Ile
NM_001349888.2:c.115T>A	NP_001336817.1:p.Phe39Ile
NM_001349889.2:c.-6T>A	NP_001336818.1:n.-6T>A
NM_001349890.2:c.-6T>A	NP_001336819.1:n.-6T>A
NM_001349891.2:c.-6T>A	NP_001336820.1:n.-6T>A
NM_001349892.2:c.-6T>A	NP_001336821.1:n.-6T>A
NM_001349893.2:c.-6T>A	NP_001336822.1:n.-6T>A
NM_178454.6:c.385T>A	NP_848549.3:p.Phe129Ile
NR_146301.2:n.519T>A
NR_146302.2:n.379T>A
NR_146303.2:n.730T>A
NR_146304.2:n.590T>A
NR_146305.2:n.573T>A
NR_146306.2:n.545T>A
NR_146307.2:n.618T>A
NR_146308.2:n.685T>A