Canonical Allele Identifier: CA1188789415

Gene: DRAM2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111120614G= , CM000663.2:g.111120614G=	GRCh38
NC_000001.10:g.111663236G= , CM000663.1:g.111663236G=	GRCh37
NC_000001.9:g.111464759G=	NCBI36
NG_053089.1:g.24603C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484310.6:c.419C= MANE Select	ENSP00000503400.1:p.Thr140=
ENST00000539140.6:c.419C=	ENSP00000437718.1:p.Thr140=
ENST00000286692.8:c.419C=	ENSP00000286692.4:p.Thr140=
ENST00000461449.5:n.193C=
ENST00000462092.5:n.740C=
ENST00000480600.6:n.435C=
ENST00000484310.5:n.663C=
ENST00000496430.6:c.*106C=	ENSP00000473779.1:n.*106C=
ENST00000539140.5:c.419C=	ENSP00000437718.1:p.Thr140=
NM_178454.4:c.419C=	NP_848549.3:p.Thr140=
XM_005270469.1:c.419C=	XP_005270526.1:p.Thr140=
XM_005270470.1:c.419C=	XP_005270527.1:p.Thr140=
XM_006710361.1:c.149C=	XP_006710424.1:p.Thr50=
XM_006710362.1:c.149C=	XP_006710425.1:p.Thr50=
XM_011540707.1:c.419C=	XP_011539009.1:p.Thr140=
XM_011540708.1:c.419C=	XP_011539010.1:p.Thr140=
NM_001349881.1:c.419C=	NP_001336810.1:p.Thr140=
NM_001349882.1:c.419C=	NP_001336811.1:p.Thr140=
NM_001349884.1:c.419C=	NP_001336813.1:p.Thr140=
NM_001349885.1:c.419C=	NP_001336814.1:p.Thr140=
NM_001349886.1:c.149C=	NP_001336815.1:p.Thr50=
NM_001349887.1:c.149C=	NP_001336816.1:p.Thr50=
NM_001349888.1:c.149C=	NP_001336817.1:p.Thr50=
NM_001349889.1:c.29C=	NP_001336818.1:p.Thr10=
NM_001349890.1:c.29C=	NP_001336819.1:p.Thr10=
NM_001349891.1:c.29C=	NP_001336820.1:p.Thr10=
NM_001349892.1:c.29C=	NP_001336821.1:p.Thr10=
NM_001349893.1:c.29C=	NP_001336822.1:p.Thr10=
NM_178454.5:c.419C=	NP_848549.3:p.Thr140=
NR_146301.1:n.676C=
NR_146302.1:n.536C=
NR_146303.1:n.887C=
NR_146304.1:n.747C=
NR_146305.1:n.730C=
NR_146306.1:n.702C=
NR_146307.1:n.775C=
NR_146308.1:n.842C=
NM_001349881.2:c.419C=	NP_001336810.1:p.Thr140=
NM_001349882.2:c.419C=	NP_001336811.1:p.Thr140=
NM_001349884.2:c.419C= MANE Select	NP_001336813.1:p.Thr140=
NM_001349885.2:c.419C=	NP_001336814.1:p.Thr140=
NM_001349886.2:c.149C=	NP_001336815.1:p.Thr50=
NM_001349887.2:c.149C=	NP_001336816.1:p.Thr50=
NM_001349888.2:c.149C=	NP_001336817.1:p.Thr50=
NM_001349889.2:c.29C=	NP_001336818.1:p.Thr10=
NM_001349890.2:c.29C=	NP_001336819.1:p.Thr10=
NM_001349891.2:c.29C=	NP_001336820.1:p.Thr10=
NM_001349892.2:c.29C=	NP_001336821.1:p.Thr10=
NM_001349893.2:c.29C=	NP_001336822.1:p.Thr10=
NM_178454.6:c.419C=	NP_848549.3:p.Thr140=
NR_146301.2:n.553C=
NR_146302.2:n.413C=
NR_146303.2:n.764C=
NR_146304.2:n.624C=
NR_146305.2:n.607C=
NR_146306.2:n.579C=
NR_146307.2:n.652C=
NR_146308.2:n.719C=