Canonical Allele Identifier: CA341818849
Gene: DRAM2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111120572T>C , CM000663.2:g.111120572T>C GRCh38
NC_000001.10:g.111663194T>C , CM000663.1:g.111663194T>C GRCh37
NC_000001.9:g.111464717T>C NCBI36
NG_053089.1:g.24645A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000484310.6:c.461A>G MANE Select ENSP00000503400.1:p.Gln154Arg
ENST00000539140.6:c.461A>G ENSP00000437718.1:p.Gln154Arg
ENST00000286692.8:c.461A>G ENSP00000286692.4:p.Gln154Arg
ENST00000461449.5:n.235A>G
ENST00000462092.5:n.782A>G
ENST00000477588.5:n.25A>G
ENST00000477769.1:n.29A>G
ENST00000480600.6:n.477A>G
ENST00000484310.5:n.705A>G
ENST00000496430.6:c.*148A>G ENSP00000473779.1:n.*148A>G
ENST00000539140.5:c.461A>G ENSP00000437718.1:p.Gln154Arg
NM_178454.4:c.461A>G NP_848549.3:p.Gln154Arg
XM_005270469.1:c.461A>G XP_005270526.1:p.Gln154Arg
XM_005270470.1:c.461A>G XP_005270527.1:p.Gln154Arg
XM_006710361.1:c.191A>G XP_006710424.1:p.Gln64Arg
XM_006710362.1:c.191A>G XP_006710425.1:p.Gln64Arg
XM_011540707.1:c.461A>G XP_011539009.1:p.Gln154Arg
XM_011540708.1:c.461A>G XP_011539010.1:p.Gln154Arg
NM_001349881.1:c.461A>G NP_001336810.1:p.Gln154Arg
NM_001349882.1:c.461A>G NP_001336811.1:p.Gln154Arg
NM_001349884.1:c.461A>G NP_001336813.1:p.Gln154Arg
NM_001349885.1:c.461A>G NP_001336814.1:p.Gln154Arg
NM_001349886.1:c.191A>G NP_001336815.1:p.Gln64Arg
NM_001349887.1:c.191A>G NP_001336816.1:p.Gln64Arg
NM_001349888.1:c.191A>G NP_001336817.1:p.Gln64Arg
NM_001349889.1:c.71A>G NP_001336818.1:p.Gln24Arg
NM_001349890.1:c.71A>G NP_001336819.1:p.Gln24Arg
NM_001349891.1:c.71A>G NP_001336820.1:p.Gln24Arg
NM_001349892.1:c.71A>G NP_001336821.1:p.Gln24Arg
NM_001349893.1:c.71A>G NP_001336822.1:p.Gln24Arg
NM_178454.5:c.461A>G NP_848549.3:p.Gln154Arg
NR_146301.1:n.718A>G
NR_146302.1:n.578A>G
NR_146303.1:n.929A>G
NR_146304.1:n.789A>G
NR_146305.1:n.772A>G
NR_146306.1:n.744A>G
NR_146307.1:n.817A>G
NR_146308.1:n.884A>G
NM_001349881.2:c.461A>G NP_001336810.1:p.Gln154Arg
NM_001349882.2:c.461A>G NP_001336811.1:p.Gln154Arg
NM_001349884.2:c.461A>G MANE Select NP_001336813.1:p.Gln154Arg
NM_001349885.2:c.461A>G NP_001336814.1:p.Gln154Arg
NM_001349886.2:c.191A>G NP_001336815.1:p.Gln64Arg
NM_001349887.2:c.191A>G NP_001336816.1:p.Gln64Arg
NM_001349888.2:c.191A>G NP_001336817.1:p.Gln64Arg
NM_001349889.2:c.71A>G NP_001336818.1:p.Gln24Arg
NM_001349890.2:c.71A>G NP_001336819.1:p.Gln24Arg
NM_001349891.2:c.71A>G NP_001336820.1:p.Gln24Arg
NM_001349892.2:c.71A>G NP_001336821.1:p.Gln24Arg
NM_001349893.2:c.71A>G NP_001336822.1:p.Gln24Arg
NM_178454.6:c.461A>G NP_848549.3:p.Gln154Arg
NR_146301.2:n.595A>G
NR_146302.2:n.455A>G
NR_146303.2:n.806A>G
NR_146304.2:n.666A>G
NR_146305.2:n.649A>G
NR_146306.2:n.621A>G
NR_146307.2:n.694A>G
NR_146308.2:n.761A>G