Canonical Allele Identifier: CA200117
Gene: DRAM2 HGNC NCBI

Linked Data

dbSNP Id: rs786205663

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111124860_111124868del , CM000663.2:g.111124860_111124868del GRCh38
NC_000001.10:g.111667482_111667490del , CM000663.1:g.111667482_111667490del GRCh37
NC_000001.9:g.111469005_111469013del NCBI36
NG_053089.1:g.20353_20361del

Transcript Alleles

HGVS Amino-acid change
ENST00000484310.6:c.217_225del MANE Select ENSP00000503400.1:p.Val73_Tyr75del
ENST00000539140.6:c.217_225del ENSP00000437718.1:p.Val73_Tyr75del
ENST00000286692.8:c.217_225del ENSP00000286692.4:p.Val73_Tyr75del
ENST00000461449.5:n.113+1363_113+1371del
ENST00000462092.5:n.538_546del
ENST00000480600.6:n.355+1363_355+1371del
ENST00000484310.5:n.461_469del
ENST00000496430.6:c.199+1363_199+1371del ENSP00000473779.1:n.199+1363_199+1371del
ENST00000539140.5:c.217_225del ENSP00000437718.1:p.Val73_Tyr75del
NM_178454.4:c.217_225del NP_848549.3:p.Val73_Tyr75del
XM_005270469.1:c.217_225del XP_005270526.1:p.Val73_Tyr75del
XM_005270470.1:c.217_225del XP_005270527.1:p.Val73_Tyr75del
XM_006710361.1:c.41+1363_41+1371del XP_006710424.1:n.41+1363_41+1371del
XM_006710362.1:c.41+1363_41+1371del XP_006710425.1:n.41+1363_41+1371del
XM_011540707.1:c.217_225del XP_011539009.1:p.Val73_Tyr75del
XM_011540708.1:c.217_225del XP_011539010.1:p.Val73_Tyr75del
NM_001349881.1:c.217_225del NP_001336810.1:p.Val73_Tyr75del
NM_001349882.1:c.217_225del NP_001336811.1:p.Val73_Tyr75del
NM_001349884.1:c.217_225del NP_001336813.1:p.Val73_Tyr75del
NM_001349885.1:c.217_225del NP_001336814.1:p.Val73_Tyr75del
NM_001349886.1:c.41+1363_41+1371del NP_001336815.1:n.41+1363_41+1371del
NM_001349887.1:c.41+1363_41+1371del NP_001336816.1:n.41+1363_41+1371del
NM_001349888.1:c.41+1363_41+1371del NP_001336817.1:n.41+1363_41+1371del
NM_001349889.1:c.-52+1363_-52+1371del NP_001336818.1:n.-52+1363_-52+1371del
NM_001349890.1:c.-52+1363_-52+1371del NP_001336819.1:n.-52+1363_-52+1371del
NM_001349891.1:c.-202_-194del NP_001336820.1:n.-202_-194del
NM_001349892.1:c.-52+1363_-52+1371del NP_001336821.1:n.-52+1363_-52+1371del
NM_001349893.1:c.-52+1363_-52+1371del NP_001336822.1:n.-52+1363_-52+1371del
NM_178454.5:c.217_225del NP_848549.3:p.Val73_Tyr75del
NR_146301.1:n.474_482del
NR_146302.1:n.456+1363_456+1371del
NR_146303.1:n.685_693del
NR_146304.1:n.667+1363_667+1371del
NR_146305.1:n.622+1363_622+1371del
NR_146306.1:n.622+1363_622+1371del
NR_146307.1:n.667+1363_667+1371del
NR_146308.1:n.640_648del
NM_001349881.2:c.217_225del NP_001336810.1:p.Val73_Tyr75del
NM_001349882.2:c.217_225del NP_001336811.1:p.Val73_Tyr75del
NM_001349884.2:c.217_225del MANE Select NP_001336813.1:p.Val73_Tyr75del
NM_001349885.2:c.217_225del NP_001336814.1:p.Val73_Tyr75del
NM_001349886.2:c.41+1363_41+1371del NP_001336815.1:n.41+1363_41+1371del
NM_001349887.2:c.41+1363_41+1371del NP_001336816.1:n.41+1363_41+1371del
NM_001349888.2:c.41+1363_41+1371del NP_001336817.1:n.41+1363_41+1371del
NM_001349889.2:c.-52+1363_-52+1371del NP_001336818.1:n.-52+1363_-52+1371del
NM_001349890.2:c.-52+1363_-52+1371del NP_001336819.1:n.-52+1363_-52+1371del
NM_001349891.2:c.-202_-194del NP_001336820.1:n.-202_-194del
NM_001349892.2:c.-52+1363_-52+1371del NP_001336821.1:n.-52+1363_-52+1371del
NM_001349893.2:c.-52+1363_-52+1371del NP_001336822.1:n.-52+1363_-52+1371del
NM_178454.6:c.217_225del NP_848549.3:p.Val73_Tyr75del
NR_146301.2:n.351_359del
NR_146302.2:n.333+1363_333+1371del
NR_146303.2:n.562_570del
NR_146304.2:n.544+1363_544+1371del
NR_146305.2:n.499+1363_499+1371del
NR_146306.2:n.499+1363_499+1371del
NR_146307.2:n.544+1363_544+1371del
NR_146308.2:n.517_525del