Canonical Allele Identifier: CA341818879

Gene: DRAM2

Linked Data

• MyVariant Identifiers: chr1:g.111663206A>G (hg19) ; chr1:g.111120584A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111120584A>G , CM000663.2:g.111120584A>G	GRCh38
NC_000001.10:g.111663206A>G , CM000663.1:g.111663206A>G	GRCh37
NC_000001.9:g.111464729A>G	NCBI36
NG_053089.1:g.24633T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484310.6:c.449T>C MANE Select	ENSP00000503400.1:p.Ile150Thr
ENST00000539140.6:c.449T>C	ENSP00000437718.1:p.Ile150Thr
ENST00000286692.8:c.449T>C	ENSP00000286692.4:p.Ile150Thr
ENST00000461449.5:n.223T>C
ENST00000462092.5:n.770T>C
ENST00000477588.5:n.13T>C
ENST00000477769.1:n.17T>C
ENST00000480600.6:n.465T>C
ENST00000484310.5:n.693T>C
ENST00000496430.6:c.*136T>C	ENSP00000473779.1:n.*136T>C
ENST00000539140.5:c.449T>C	ENSP00000437718.1:p.Ile150Thr
NM_178454.4:c.449T>C	NP_848549.3:p.Ile150Thr
XM_005270469.1:c.449T>C	XP_005270526.1:p.Ile150Thr
XM_005270470.1:c.449T>C	XP_005270527.1:p.Ile150Thr
XM_006710361.1:c.179T>C	XP_006710424.1:p.Ile60Thr
XM_006710362.1:c.179T>C	XP_006710425.1:p.Ile60Thr
XM_011540707.1:c.449T>C	XP_011539009.1:p.Ile150Thr
XM_011540708.1:c.449T>C	XP_011539010.1:p.Ile150Thr
NM_001349881.1:c.449T>C	NP_001336810.1:p.Ile150Thr
NM_001349882.1:c.449T>C	NP_001336811.1:p.Ile150Thr
NM_001349884.1:c.449T>C	NP_001336813.1:p.Ile150Thr
NM_001349885.1:c.449T>C	NP_001336814.1:p.Ile150Thr
NM_001349886.1:c.179T>C	NP_001336815.1:p.Ile60Thr
NM_001349887.1:c.179T>C	NP_001336816.1:p.Ile60Thr
NM_001349888.1:c.179T>C	NP_001336817.1:p.Ile60Thr
NM_001349889.1:c.59T>C	NP_001336818.1:p.Ile20Thr
NM_001349890.1:c.59T>C	NP_001336819.1:p.Ile20Thr
NM_001349891.1:c.59T>C	NP_001336820.1:p.Ile20Thr
NM_001349892.1:c.59T>C	NP_001336821.1:p.Ile20Thr
NM_001349893.1:c.59T>C	NP_001336822.1:p.Ile20Thr
NM_178454.5:c.449T>C	NP_848549.3:p.Ile150Thr
NR_146301.1:n.706T>C
NR_146302.1:n.566T>C
NR_146303.1:n.917T>C
NR_146304.1:n.777T>C
NR_146305.1:n.760T>C
NR_146306.1:n.732T>C
NR_146307.1:n.805T>C
NR_146308.1:n.872T>C
NM_001349881.2:c.449T>C	NP_001336810.1:p.Ile150Thr
NM_001349882.2:c.449T>C	NP_001336811.1:p.Ile150Thr
NM_001349884.2:c.449T>C MANE Select	NP_001336813.1:p.Ile150Thr
NM_001349885.2:c.449T>C	NP_001336814.1:p.Ile150Thr
NM_001349886.2:c.179T>C	NP_001336815.1:p.Ile60Thr
NM_001349887.2:c.179T>C	NP_001336816.1:p.Ile60Thr
NM_001349888.2:c.179T>C	NP_001336817.1:p.Ile60Thr
NM_001349889.2:c.59T>C	NP_001336818.1:p.Ile20Thr
NM_001349890.2:c.59T>C	NP_001336819.1:p.Ile20Thr
NM_001349891.2:c.59T>C	NP_001336820.1:p.Ile20Thr
NM_001349892.2:c.59T>C	NP_001336821.1:p.Ile20Thr
NM_001349893.2:c.59T>C	NP_001336822.1:p.Ile20Thr
NM_178454.6:c.449T>C	NP_848549.3:p.Ile150Thr
NR_146301.2:n.583T>C
NR_146302.2:n.443T>C
NR_146303.2:n.794T>C
NR_146304.2:n.654T>C
NR_146305.2:n.637T>C
NR_146306.2:n.609T>C
NR_146307.2:n.682T>C
NR_146308.2:n.749T>C