Canonical Allele Identifier: CA341818774
Gene: DRAM2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111120538C>T , CM000663.2:g.111120538C>T GRCh38
NC_000001.10:g.111663160C>T , CM000663.1:g.111663160C>T GRCh37
NC_000001.9:g.111464683C>T NCBI36
NG_053089.1:g.24679G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000484310.6:c.495G>A MANE Select ENSP00000503400.1:p.Trp165Ter
ENST00000539140.6:c.495G>A ENSP00000437718.1:p.Trp165Ter
ENST00000286692.8:c.495G>A ENSP00000286692.4:p.Trp165Ter
ENST00000461449.5:n.269G>A
ENST00000477588.5:n.59G>A
ENST00000477769.1:n.63G>A
ENST00000480600.6:n.511G>A
ENST00000484310.5:n.739G>A
ENST00000496430.6:c.*182G>A ENSP00000473779.1:n.*182G>A
ENST00000539140.5:c.495G>A ENSP00000437718.1:p.Trp165Ter
NM_178454.4:c.495G>A NP_848549.3:p.Trp165Ter
XM_005270469.1:c.495G>A XP_005270526.1:p.Trp165Ter
XM_005270470.1:c.495G>A XP_005270527.1:p.Trp165Ter
XM_006710361.1:c.225G>A XP_006710424.1:p.Trp75Ter
XM_006710362.1:c.225G>A XP_006710425.1:p.Trp75Ter
XM_011540707.1:c.495G>A XP_011539009.1:p.Trp165Ter
XM_011540708.1:c.495G>A XP_011539010.1:p.Trp165Ter
NM_001349881.1:c.495G>A NP_001336810.1:p.Trp165Ter
NM_001349882.1:c.495G>A NP_001336811.1:p.Trp165Ter
NM_001349884.1:c.495G>A NP_001336813.1:p.Trp165Ter
NM_001349885.1:c.495G>A NP_001336814.1:p.Trp165Ter
NM_001349886.1:c.225G>A NP_001336815.1:p.Trp75Ter
NM_001349887.1:c.225G>A NP_001336816.1:p.Trp75Ter
NM_001349888.1:c.225G>A NP_001336817.1:p.Trp75Ter
NM_001349889.1:c.105G>A NP_001336818.1:p.Trp35Ter
NM_001349890.1:c.105G>A NP_001336819.1:p.Trp35Ter
NM_001349891.1:c.105G>A NP_001336820.1:p.Trp35Ter
NM_001349892.1:c.105G>A NP_001336821.1:p.Trp35Ter
NM_001349893.1:c.105G>A NP_001336822.1:p.Trp35Ter
NM_178454.5:c.495G>A NP_848549.3:p.Trp165Ter
NR_146301.1:n.752G>A
NR_146302.1:n.612G>A
NR_146303.1:n.963G>A
NR_146304.1:n.823G>A
NR_146305.1:n.806G>A
NR_146306.1:n.778G>A
NR_146307.1:n.851G>A
NR_146308.1:n.918G>A
NM_001349881.2:c.495G>A NP_001336810.1:p.Trp165Ter
NM_001349882.2:c.495G>A NP_001336811.1:p.Trp165Ter
NM_001349884.2:c.495G>A MANE Select NP_001336813.1:p.Trp165Ter
NM_001349885.2:c.495G>A NP_001336814.1:p.Trp165Ter
NM_001349886.2:c.225G>A NP_001336815.1:p.Trp75Ter
NM_001349887.2:c.225G>A NP_001336816.1:p.Trp75Ter
NM_001349888.2:c.225G>A NP_001336817.1:p.Trp75Ter
NM_001349889.2:c.105G>A NP_001336818.1:p.Trp35Ter
NM_001349890.2:c.105G>A NP_001336819.1:p.Trp35Ter
NM_001349891.2:c.105G>A NP_001336820.1:p.Trp35Ter
NM_001349892.2:c.105G>A NP_001336821.1:p.Trp35Ter
NM_001349893.2:c.105G>A NP_001336822.1:p.Trp35Ter
NM_178454.6:c.495G>A NP_848549.3:p.Trp165Ter
NR_146301.2:n.629G>A
NR_146302.2:n.489G>A
NR_146303.2:n.840G>A
NR_146304.2:n.700G>A
NR_146305.2:n.683G>A
NR_146306.2:n.655G>A
NR_146307.2:n.728G>A
NR_146308.2:n.795G>A