Canonical Allele Identifier: CA916262712

Gene: DRAM2

Linked Data

• dbSNP Id: rs1571017918
• gnomAD v3: 1-111120754-ACATTTAAAAGCACAACC-A
• gnomAD v4: 1-111120754-ACATTTAAAAGCACAACC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111120757_111120773del , CM000663.2:g.111120757_111120773del	GRCh38
NC_000001.10:g.111663379_111663395del , CM000663.1:g.111663379_111663395del	GRCh37
NC_000001.9:g.111464902_111464918del	NCBI36
NG_053089.1:g.24446_24462del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484310.6:c.340-78_340-62del MANE Select	ENSP00000503400.1:n.340-78_340-62del
ENST00000539140.6:c.340-78_340-62del	ENSP00000437718.1:n.340-78_340-62del
ENST00000286692.8:c.340-78_340-62del	ENSP00000286692.4:n.340-78_340-62del
ENST00000461449.5:n.114-78_114-62del
ENST00000462092.5:n.661-78_661-62del
ENST00000480600.6:n.356-78_356-62del
ENST00000484310.5:n.584-78_584-62del
ENST00000496430.6:c.*27-78_*27-62del	ENSP00000473779.1:n.*27-78_*27-62del
ENST00000539140.5:c.340-78_340-62del	ENSP00000437718.1:n.340-78_340-62del
NM_178454.4:c.340-78_340-62del	NP_848549.3:n.340-78_340-62del
XM_005270469.1:c.340-78_340-62del	XP_005270526.1:n.340-78_340-62del
XM_005270470.1:c.340-78_340-62del	XP_005270527.1:n.340-78_340-62del
XM_006710361.1:c.70-78_70-62del	XP_006710424.1:n.70-78_70-62del
XM_006710362.1:c.70-78_70-62del	XP_006710425.1:n.70-78_70-62del
XM_011540707.1:c.340-78_340-62del	XP_011539009.1:n.340-78_340-62del
XM_011540708.1:c.340-78_340-62del	XP_011539010.1:n.340-78_340-62del
NM_001349881.1:c.340-78_340-62del	NP_001336810.1:n.340-78_340-62del
NM_001349882.1:c.340-78_340-62del	NP_001336811.1:n.340-78_340-62del
NM_001349884.1:c.340-78_340-62del	NP_001336813.1:n.340-78_340-62del
NM_001349885.1:c.340-78_340-62del	NP_001336814.1:n.340-78_340-62del
NM_001349886.1:c.70-78_70-62del	NP_001336815.1:n.70-78_70-62del
NM_001349887.1:c.70-78_70-62del	NP_001336816.1:n.70-78_70-62del
NM_001349888.1:c.70-78_70-62del	NP_001336817.1:n.70-78_70-62del
NM_001349889.1:c.-51-78_-51-62del	NP_001336818.1:n.-51-78_-51-62del
NM_001349890.1:c.-51-78_-51-62del	NP_001336819.1:n.-51-78_-51-62del
NM_001349891.1:c.-51-78_-51-62del	NP_001336820.1:n.-51-78_-51-62del
NM_001349892.1:c.-51-78_-51-62del	NP_001336821.1:n.-51-78_-51-62del
NM_001349893.1:c.-51-78_-51-62del	NP_001336822.1:n.-51-78_-51-62del
NM_178454.5:c.340-78_340-62del	NP_848549.3:n.340-78_340-62del
NR_146301.1:n.597-78_597-62del
NR_146302.1:n.457-78_457-62del
NR_146303.1:n.808-78_808-62del
NR_146304.1:n.668-78_668-62del
NR_146305.1:n.651-78_651-62del
NR_146306.1:n.623-78_623-62del
NR_146307.1:n.696-78_696-62del
NR_146308.1:n.763-78_763-62del
NM_001349881.2:c.340-78_340-62del	NP_001336810.1:n.340-78_340-62del
NM_001349882.2:c.340-78_340-62del	NP_001336811.1:n.340-78_340-62del
NM_001349884.2:c.340-78_340-62del MANE Select	NP_001336813.1:n.340-78_340-62del
NM_001349885.2:c.340-78_340-62del	NP_001336814.1:n.340-78_340-62del
NM_001349886.2:c.70-78_70-62del	NP_001336815.1:n.70-78_70-62del
NM_001349887.2:c.70-78_70-62del	NP_001336816.1:n.70-78_70-62del
NM_001349888.2:c.70-78_70-62del	NP_001336817.1:n.70-78_70-62del
NM_001349889.2:c.-51-78_-51-62del	NP_001336818.1:n.-51-78_-51-62del
NM_001349890.2:c.-51-78_-51-62del	NP_001336819.1:n.-51-78_-51-62del
NM_001349891.2:c.-51-78_-51-62del	NP_001336820.1:n.-51-78_-51-62del
NM_001349892.2:c.-51-78_-51-62del	NP_001336821.1:n.-51-78_-51-62del
NM_001349893.2:c.-51-78_-51-62del	NP_001336822.1:n.-51-78_-51-62del
NM_178454.6:c.340-78_340-62del	NP_848549.3:n.340-78_340-62del
NR_146301.2:n.474-78_474-62del
NR_146302.2:n.334-78_334-62del
NR_146303.2:n.685-78_685-62del
NR_146304.2:n.545-78_545-62del
NR_146305.2:n.528-78_528-62del
NR_146306.2:n.500-78_500-62del
NR_146307.2:n.573-78_573-62del
NR_146308.2:n.640-78_640-62del