Canonical Allele Identifier: CA341818970

Gene: DRAM2

Linked Data

• gnomAD v4: 1-111120624-A-G
• MyVariant Identifiers: chr1:g.111663246A>G (hg19) ; chr1:g.111120624A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111120624A>G , CM000663.2:g.111120624A>G	GRCh38
NC_000001.10:g.111663246A>G , CM000663.1:g.111663246A>G	GRCh37
NC_000001.9:g.111464769A>G	NCBI36
NG_053089.1:g.24593T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484310.6:c.409T>C MANE Select	ENSP00000503400.1:p.Phe137Leu
ENST00000539140.6:c.409T>C	ENSP00000437718.1:p.Phe137Leu
ENST00000286692.8:c.409T>C	ENSP00000286692.4:p.Phe137Leu
ENST00000461449.5:n.183T>C
ENST00000462092.5:n.730T>C
ENST00000480600.6:n.425T>C
ENST00000484310.5:n.653T>C
ENST00000496430.6:c.*96T>C	ENSP00000473779.1:n.*96T>C
ENST00000539140.5:c.409T>C	ENSP00000437718.1:p.Phe137Leu
NM_178454.4:c.409T>C	NP_848549.3:p.Phe137Leu
XM_005270469.1:c.409T>C	XP_005270526.1:p.Phe137Leu
XM_005270470.1:c.409T>C	XP_005270527.1:p.Phe137Leu
XM_006710361.1:c.139T>C	XP_006710424.1:p.Phe47Leu
XM_006710362.1:c.139T>C	XP_006710425.1:p.Phe47Leu
XM_011540707.1:c.409T>C	XP_011539009.1:p.Phe137Leu
XM_011540708.1:c.409T>C	XP_011539010.1:p.Phe137Leu
NM_001349881.1:c.409T>C	NP_001336810.1:p.Phe137Leu
NM_001349882.1:c.409T>C	NP_001336811.1:p.Phe137Leu
NM_001349884.1:c.409T>C	NP_001336813.1:p.Phe137Leu
NM_001349885.1:c.409T>C	NP_001336814.1:p.Phe137Leu
NM_001349886.1:c.139T>C	NP_001336815.1:p.Phe47Leu
NM_001349887.1:c.139T>C	NP_001336816.1:p.Phe47Leu
NM_001349888.1:c.139T>C	NP_001336817.1:p.Phe47Leu
NM_001349889.1:c.19T>C	NP_001336818.1:p.Phe7Leu
NM_001349890.1:c.19T>C	NP_001336819.1:p.Phe7Leu
NM_001349891.1:c.19T>C	NP_001336820.1:p.Phe7Leu
NM_001349892.1:c.19T>C	NP_001336821.1:p.Phe7Leu
NM_001349893.1:c.19T>C	NP_001336822.1:p.Phe7Leu
NM_178454.5:c.409T>C	NP_848549.3:p.Phe137Leu
NR_146301.1:n.666T>C
NR_146302.1:n.526T>C
NR_146303.1:n.877T>C
NR_146304.1:n.737T>C
NR_146305.1:n.720T>C
NR_146306.1:n.692T>C
NR_146307.1:n.765T>C
NR_146308.1:n.832T>C
NM_001349881.2:c.409T>C	NP_001336810.1:p.Phe137Leu
NM_001349882.2:c.409T>C	NP_001336811.1:p.Phe137Leu
NM_001349884.2:c.409T>C MANE Select	NP_001336813.1:p.Phe137Leu
NM_001349885.2:c.409T>C	NP_001336814.1:p.Phe137Leu
NM_001349886.2:c.139T>C	NP_001336815.1:p.Phe47Leu
NM_001349887.2:c.139T>C	NP_001336816.1:p.Phe47Leu
NM_001349888.2:c.139T>C	NP_001336817.1:p.Phe47Leu
NM_001349889.2:c.19T>C	NP_001336818.1:p.Phe7Leu
NM_001349890.2:c.19T>C	NP_001336819.1:p.Phe7Leu
NM_001349891.2:c.19T>C	NP_001336820.1:p.Phe7Leu
NM_001349892.2:c.19T>C	NP_001336821.1:p.Phe7Leu
NM_001349893.2:c.19T>C	NP_001336822.1:p.Phe7Leu
NM_178454.6:c.409T>C	NP_848549.3:p.Phe137Leu
NR_146301.2:n.543T>C
NR_146302.2:n.403T>C
NR_146303.2:n.754T>C
NR_146304.2:n.614T>C
NR_146305.2:n.597T>C
NR_146306.2:n.569T>C
NR_146307.2:n.642T>C
NR_146308.2:n.709T>C