Canonical Allele Identifier: CA341819048

Gene: DRAM2

Linked Data

• MyVariant Identifiers: chr1:g.111663281G>A (hg19) ; chr1:g.111120659G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111120659G>A , CM000663.2:g.111120659G>A	GRCh38
NC_000001.10:g.111663281G>A , CM000663.1:g.111663281G>A	GRCh37
NC_000001.9:g.111464804G>A	NCBI36
NG_053089.1:g.24558C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484310.6:c.374C>T MANE Select	ENSP00000503400.1:p.Ala125Val
ENST00000539140.6:c.374C>T	ENSP00000437718.1:p.Ala125Val
ENST00000286692.8:c.374C>T	ENSP00000286692.4:p.Ala125Val
ENST00000461449.5:n.148C>T
ENST00000462092.5:n.695C>T
ENST00000480600.6:n.390C>T
ENST00000484310.5:n.618C>T
ENST00000496430.6:c.*61C>T	ENSP00000473779.1:n.*61C>T
ENST00000539140.5:c.374C>T	ENSP00000437718.1:p.Ala125Val
NM_178454.4:c.374C>T	NP_848549.3:p.Ala125Val
XM_005270469.1:c.374C>T	XP_005270526.1:p.Ala125Val
XM_005270470.1:c.374C>T	XP_005270527.1:p.Ala125Val
XM_006710361.1:c.104C>T	XP_006710424.1:p.Ala35Val
XM_006710362.1:c.104C>T	XP_006710425.1:p.Ala35Val
XM_011540707.1:c.374C>T	XP_011539009.1:p.Ala125Val
XM_011540708.1:c.374C>T	XP_011539010.1:p.Ala125Val
NM_001349881.1:c.374C>T	NP_001336810.1:p.Ala125Val
NM_001349882.1:c.374C>T	NP_001336811.1:p.Ala125Val
NM_001349884.1:c.374C>T	NP_001336813.1:p.Ala125Val
NM_001349885.1:c.374C>T	NP_001336814.1:p.Ala125Val
NM_001349886.1:c.104C>T	NP_001336815.1:p.Ala35Val
NM_001349887.1:c.104C>T	NP_001336816.1:p.Ala35Val
NM_001349888.1:c.104C>T	NP_001336817.1:p.Ala35Val
NM_001349889.1:c.-17C>T	NP_001336818.1:n.-17C>T
NM_001349890.1:c.-17C>T	NP_001336819.1:n.-17C>T
NM_001349891.1:c.-17C>T	NP_001336820.1:n.-17C>T
NM_001349892.1:c.-17C>T	NP_001336821.1:n.-17C>T
NM_001349893.1:c.-17C>T	NP_001336822.1:n.-17C>T
NM_178454.5:c.374C>T	NP_848549.3:p.Ala125Val
NR_146301.1:n.631C>T
NR_146302.1:n.491C>T
NR_146303.1:n.842C>T
NR_146304.1:n.702C>T
NR_146305.1:n.685C>T
NR_146306.1:n.657C>T
NR_146307.1:n.730C>T
NR_146308.1:n.797C>T
NM_001349881.2:c.374C>T	NP_001336810.1:p.Ala125Val
NM_001349882.2:c.374C>T	NP_001336811.1:p.Ala125Val
NM_001349884.2:c.374C>T MANE Select	NP_001336813.1:p.Ala125Val
NM_001349885.2:c.374C>T	NP_001336814.1:p.Ala125Val
NM_001349886.2:c.104C>T	NP_001336815.1:p.Ala35Val
NM_001349887.2:c.104C>T	NP_001336816.1:p.Ala35Val
NM_001349888.2:c.104C>T	NP_001336817.1:p.Ala35Val
NM_001349889.2:c.-17C>T	NP_001336818.1:n.-17C>T
NM_001349890.2:c.-17C>T	NP_001336819.1:n.-17C>T
NM_001349891.2:c.-17C>T	NP_001336820.1:n.-17C>T
NM_001349892.2:c.-17C>T	NP_001336821.1:n.-17C>T
NM_001349893.2:c.-17C>T	NP_001336822.1:n.-17C>T
NM_178454.6:c.374C>T	NP_848549.3:p.Ala125Val
NR_146301.2:n.508C>T
NR_146302.2:n.368C>T
NR_146303.2:n.719C>T
NR_146304.2:n.579C>T
NR_146305.2:n.562C>T
NR_146306.2:n.534C>T
NR_146307.2:n.607C>T
NR_146308.2:n.674C>T