Canonical Allele Identifier: CA1188789441

Gene: DRAM2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111120678_111120679delinsCA , CM000663.2:g.111120678_111120679delinsCA	GRCh38
NC_000001.10:g.111663300_111663301delinsCA , CM000663.1:g.111663300_111663301delinsCA	GRCh37
NC_000001.9:g.111464823_111464824delinsCA	NCBI36
NG_053089.1:g.24538_24539delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484310.6:c.354_355delinsTG MANE Select	ENSP00000503400.1:p.Phe118=
ENST00000539140.6:c.354_355delinsTG	ENSP00000437718.1:p.Phe118=
ENST00000286692.8:c.354_355delinsTG	ENSP00000286692.4:p.Phe118=
ENST00000461449.5:n.128_129delinsTG
ENST00000462092.5:n.675_676delinsTG
ENST00000480600.6:n.370_371delinsTG
ENST00000484310.5:n.598_599delinsTG
ENST00000496430.6:c.*41_*42delinsTG	ENSP00000473779.1:n.*41_*42delinsTG
ENST00000539140.5:c.354_355delinsTG	ENSP00000437718.1:p.Phe118=
NM_178454.4:c.354_355delinsTG	NP_848549.3:p.Phe118=
XM_005270469.1:c.354_355delinsTG	XP_005270526.1:p.Phe118=
XM_005270470.1:c.354_355delinsTG	XP_005270527.1:p.Phe118=
XM_006710361.1:c.84_85delinsTG	XP_006710424.1:p.Phe28=
XM_006710362.1:c.84_85delinsTG	XP_006710425.1:p.Phe28=
XM_011540707.1:c.354_355delinsTG	XP_011539009.1:p.Phe118=
XM_011540708.1:c.354_355delinsTG	XP_011539010.1:p.Phe118=
NM_001349881.1:c.354_355delinsTG	NP_001336810.1:p.Phe118=
NM_001349882.1:c.354_355delinsTG	NP_001336811.1:p.Phe118=
NM_001349884.1:c.354_355delinsTG	NP_001336813.1:p.Phe118=
NM_001349885.1:c.354_355delinsTG	NP_001336814.1:p.Phe118=
NM_001349886.1:c.84_85delinsTG	NP_001336815.1:p.Phe28=
NM_001349887.1:c.84_85delinsTG	NP_001336816.1:p.Phe28=
NM_001349888.1:c.84_85delinsTG	NP_001336817.1:p.Phe28=
NM_001349889.1:c.-37_-36delinsTG	NP_001336818.1:n.-37_-36delinsTG
NM_001349890.1:c.-37_-36delinsTG	NP_001336819.1:n.-37_-36delinsTG
NM_001349891.1:c.-37_-36delinsTG	NP_001336820.1:n.-37_-36delinsTG
NM_001349892.1:c.-37_-36delinsTG	NP_001336821.1:n.-37_-36delinsTG
NM_001349893.1:c.-37_-36delinsTG	NP_001336822.1:n.-37_-36delinsTG
NM_178454.5:c.354_355delinsTG	NP_848549.3:p.Phe118=
NR_146301.1:n.611_612delinsTG
NR_146302.1:n.471_472delinsTG
NR_146303.1:n.822_823delinsTG
NR_146304.1:n.682_683delinsTG
NR_146305.1:n.665_666delinsTG
NR_146306.1:n.637_638delinsTG
NR_146307.1:n.710_711delinsTG
NR_146308.1:n.777_778delinsTG
NM_001349881.2:c.354_355delinsTG	NP_001336810.1:p.Phe118=
NM_001349882.2:c.354_355delinsTG	NP_001336811.1:p.Phe118=
NM_001349884.2:c.354_355delinsTG MANE Select	NP_001336813.1:p.Phe118=
NM_001349885.2:c.354_355delinsTG	NP_001336814.1:p.Phe118=
NM_001349886.2:c.84_85delinsTG	NP_001336815.1:p.Phe28=
NM_001349887.2:c.84_85delinsTG	NP_001336816.1:p.Phe28=
NM_001349888.2:c.84_85delinsTG	NP_001336817.1:p.Phe28=
NM_001349889.2:c.-37_-36delinsTG	NP_001336818.1:n.-37_-36delinsTG
NM_001349890.2:c.-37_-36delinsTG	NP_001336819.1:n.-37_-36delinsTG
NM_001349891.2:c.-37_-36delinsTG	NP_001336820.1:n.-37_-36delinsTG
NM_001349892.2:c.-37_-36delinsTG	NP_001336821.1:n.-37_-36delinsTG
NM_001349893.2:c.-37_-36delinsTG	NP_001336822.1:n.-37_-36delinsTG
NM_178454.6:c.354_355delinsTG	NP_848549.3:p.Phe118=
NR_146301.2:n.488_489delinsTG
NR_146302.2:n.348_349delinsTG
NR_146303.2:n.699_700delinsTG
NR_146304.2:n.559_560delinsTG
NR_146305.2:n.542_543delinsTG
NR_146306.2:n.514_515delinsTG
NR_146307.2:n.587_588delinsTG
NR_146308.2:n.654_655delinsTG