Canonical Allele Identifier: CA341818944

Gene: DRAM2

Linked Data

• MyVariant Identifiers: chr1:g.111663234T>C (hg19) ; chr1:g.111120612T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111120612T>C , CM000663.2:g.111120612T>C	GRCh38
NC_000001.10:g.111663234T>C , CM000663.1:g.111663234T>C	GRCh37
NC_000001.9:g.111464757T>C	NCBI36
NG_053089.1:g.24605A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484310.6:c.421A>G MANE Select	ENSP00000503400.1:p.Ile141Val
ENST00000539140.6:c.421A>G	ENSP00000437718.1:p.Ile141Val
ENST00000286692.8:c.421A>G	ENSP00000286692.4:p.Ile141Val
ENST00000461449.5:n.195A>G
ENST00000462092.5:n.742A>G
ENST00000480600.6:n.437A>G
ENST00000484310.5:n.665A>G
ENST00000496430.6:c.*108A>G	ENSP00000473779.1:n.*108A>G
ENST00000539140.5:c.421A>G	ENSP00000437718.1:p.Ile141Val
NM_178454.4:c.421A>G	NP_848549.3:p.Ile141Val
XM_005270469.1:c.421A>G	XP_005270526.1:p.Ile141Val
XM_005270470.1:c.421A>G	XP_005270527.1:p.Ile141Val
XM_006710361.1:c.151A>G	XP_006710424.1:p.Ile51Val
XM_006710362.1:c.151A>G	XP_006710425.1:p.Ile51Val
XM_011540707.1:c.421A>G	XP_011539009.1:p.Ile141Val
XM_011540708.1:c.421A>G	XP_011539010.1:p.Ile141Val
NM_001349881.1:c.421A>G	NP_001336810.1:p.Ile141Val
NM_001349882.1:c.421A>G	NP_001336811.1:p.Ile141Val
NM_001349884.1:c.421A>G	NP_001336813.1:p.Ile141Val
NM_001349885.1:c.421A>G	NP_001336814.1:p.Ile141Val
NM_001349886.1:c.151A>G	NP_001336815.1:p.Ile51Val
NM_001349887.1:c.151A>G	NP_001336816.1:p.Ile51Val
NM_001349888.1:c.151A>G	NP_001336817.1:p.Ile51Val
NM_001349889.1:c.31A>G	NP_001336818.1:p.Ile11Val
NM_001349890.1:c.31A>G	NP_001336819.1:p.Ile11Val
NM_001349891.1:c.31A>G	NP_001336820.1:p.Ile11Val
NM_001349892.1:c.31A>G	NP_001336821.1:p.Ile11Val
NM_001349893.1:c.31A>G	NP_001336822.1:p.Ile11Val
NM_178454.5:c.421A>G	NP_848549.3:p.Ile141Val
NR_146301.1:n.678A>G
NR_146302.1:n.538A>G
NR_146303.1:n.889A>G
NR_146304.1:n.749A>G
NR_146305.1:n.732A>G
NR_146306.1:n.704A>G
NR_146307.1:n.777A>G
NR_146308.1:n.844A>G
NM_001349881.2:c.421A>G	NP_001336810.1:p.Ile141Val
NM_001349882.2:c.421A>G	NP_001336811.1:p.Ile141Val
NM_001349884.2:c.421A>G MANE Select	NP_001336813.1:p.Ile141Val
NM_001349885.2:c.421A>G	NP_001336814.1:p.Ile141Val
NM_001349886.2:c.151A>G	NP_001336815.1:p.Ile51Val
NM_001349887.2:c.151A>G	NP_001336816.1:p.Ile51Val
NM_001349888.2:c.151A>G	NP_001336817.1:p.Ile51Val
NM_001349889.2:c.31A>G	NP_001336818.1:p.Ile11Val
NM_001349890.2:c.31A>G	NP_001336819.1:p.Ile11Val
NM_001349891.2:c.31A>G	NP_001336820.1:p.Ile11Val
NM_001349892.2:c.31A>G	NP_001336821.1:p.Ile11Val
NM_001349893.2:c.31A>G	NP_001336822.1:p.Ile11Val
NM_178454.6:c.421A>G	NP_848549.3:p.Ile141Val
NR_146301.2:n.555A>G
NR_146302.2:n.415A>G
NR_146303.2:n.766A>G
NR_146304.2:n.626A>G
NR_146305.2:n.609A>G
NR_146306.2:n.581A>G
NR_146307.2:n.654A>G
NR_146308.2:n.721A>G