Canonical Allele Identifier: CA2580060801

Gene: DRAM2

Linked Data

• ClinVar Variation Id: 2003336
• ClinVar RCV Id: RCV002825254

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111120592_111120593delinsGG , CM000663.2:g.111120592_111120593delinsGG	GRCh38
NC_000001.10:g.111663214_111663215delinsGG , CM000663.1:g.111663214_111663215delinsGG	GRCh37
NC_000001.9:g.111464737_111464738delinsGG	NCBI36
NG_053089.1:g.24624_24625delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484310.6:c.440_441delinsCC MANE Select	ENSP00000503400.1:p.Gln147Pro
ENST00000539140.6:c.440_441delinsCC	ENSP00000437718.1:p.Gln147Pro
ENST00000286692.8:c.440_441delinsCC	ENSP00000286692.4:p.Gln147Pro
ENST00000461449.5:n.214_215delinsCC
ENST00000462092.5:n.761_762delinsCC
ENST00000477588.5:n.4_5delinsCC
ENST00000477769.1:n.8_9delinsCC
ENST00000480600.6:n.456_457delinsCC
ENST00000484310.5:n.684_685delinsCC
ENST00000496430.6:c.*127_*128delinsCC	ENSP00000473779.1:n.*127_*128delinsCC
ENST00000539140.5:c.440_441delinsCC	ENSP00000437718.1:p.Gln147Pro
NM_178454.4:c.440_441delinsCC	NP_848549.3:p.Gln147Pro
XM_005270469.1:c.440_441delinsCC	XP_005270526.1:p.Gln147Pro
XM_005270470.1:c.440_441delinsCC	XP_005270527.1:p.Gln147Pro
XM_006710361.1:c.170_171delinsCC	XP_006710424.1:p.Gln57Pro
XM_006710362.1:c.170_171delinsCC	XP_006710425.1:p.Gln57Pro
XM_011540707.1:c.440_441delinsCC	XP_011539009.1:p.Gln147Pro
XM_011540708.1:c.440_441delinsCC	XP_011539010.1:p.Gln147Pro
NM_001349881.1:c.440_441delinsCC	NP_001336810.1:p.Gln147Pro
NM_001349882.1:c.440_441delinsCC	NP_001336811.1:p.Gln147Pro
NM_001349884.1:c.440_441delinsCC	NP_001336813.1:p.Gln147Pro
NM_001349885.1:c.440_441delinsCC	NP_001336814.1:p.Gln147Pro
NM_001349886.1:c.170_171delinsCC	NP_001336815.1:p.Gln57Pro
NM_001349887.1:c.170_171delinsCC	NP_001336816.1:p.Gln57Pro
NM_001349888.1:c.170_171delinsCC	NP_001336817.1:p.Gln57Pro
NM_001349889.1:c.50_51delinsCC	NP_001336818.1:p.Gln17Pro
NM_001349890.1:c.50_51delinsCC	NP_001336819.1:p.Gln17Pro
NM_001349891.1:c.50_51delinsCC	NP_001336820.1:p.Gln17Pro
NM_001349892.1:c.50_51delinsCC	NP_001336821.1:p.Gln17Pro
NM_001349893.1:c.50_51delinsCC	NP_001336822.1:p.Gln17Pro
NM_178454.5:c.440_441delinsCC	NP_848549.3:p.Gln147Pro
NR_146301.1:n.697_698delinsCC
NR_146302.1:n.557_558delinsCC
NR_146303.1:n.908_909delinsCC
NR_146304.1:n.768_769delinsCC
NR_146305.1:n.751_752delinsCC
NR_146306.1:n.723_724delinsCC
NR_146307.1:n.796_797delinsCC
NR_146308.1:n.863_864delinsCC
NM_001349881.2:c.440_441delinsCC	NP_001336810.1:p.Gln147Pro
NM_001349882.2:c.440_441delinsCC	NP_001336811.1:p.Gln147Pro
NM_001349884.2:c.440_441delinsCC MANE Select	NP_001336813.1:p.Gln147Pro
NM_001349885.2:c.440_441delinsCC	NP_001336814.1:p.Gln147Pro
NM_001349886.2:c.170_171delinsCC	NP_001336815.1:p.Gln57Pro
NM_001349887.2:c.170_171delinsCC	NP_001336816.1:p.Gln57Pro
NM_001349888.2:c.170_171delinsCC	NP_001336817.1:p.Gln57Pro
NM_001349889.2:c.50_51delinsCC	NP_001336818.1:p.Gln17Pro
NM_001349890.2:c.50_51delinsCC	NP_001336819.1:p.Gln17Pro
NM_001349891.2:c.50_51delinsCC	NP_001336820.1:p.Gln17Pro
NM_001349892.2:c.50_51delinsCC	NP_001336821.1:p.Gln17Pro
NM_001349893.2:c.50_51delinsCC	NP_001336822.1:p.Gln17Pro
NM_178454.6:c.440_441delinsCC	NP_848549.3:p.Gln147Pro
NR_146301.2:n.574_575delinsCC
NR_146302.2:n.434_435delinsCC
NR_146303.2:n.785_786delinsCC
NR_146304.2:n.645_646delinsCC
NR_146305.2:n.628_629delinsCC
NR_146306.2:n.600_601delinsCC
NR_146307.2:n.673_674delinsCC
NR_146308.2:n.740_741delinsCC