Canonical Allele Identifier: CA419621354

Gene: DRAM2

Linked Data

• MyVariant Identifiers: chr1:g.111663211G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111120589G>C , CM000663.2:g.111120589G>C	GRCh38
NC_000001.10:g.111663211G>C , CM000663.1:g.111663211G>C	GRCh37
NC_000001.9:g.111464734G>C	NCBI36
NG_053089.1:g.24628C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484310.6:c.444C>G MANE Select	ENSP00000503400.1:p.Pro148=
ENST00000539140.6:c.444C>G	ENSP00000437718.1:p.Pro148=
ENST00000286692.8:c.444C>G	ENSP00000286692.4:p.Pro148=
ENST00000461449.5:n.218C>G
ENST00000462092.5:n.765C>G
ENST00000477588.5:n.8C>G
ENST00000477769.1:n.12C>G
ENST00000480600.6:n.460C>G
ENST00000484310.5:n.688C>G
ENST00000496430.6:c.*131C>G	ENSP00000473779.1:n.*131C>G
ENST00000539140.5:c.444C>G	ENSP00000437718.1:p.Pro148=
NM_178454.4:c.444C>G	NP_848549.3:p.Pro148=
XM_005270469.1:c.444C>G	XP_005270526.1:p.Pro148=
XM_005270470.1:c.444C>G	XP_005270527.1:p.Pro148=
XM_006710361.1:c.174C>G	XP_006710424.1:p.Pro58=
XM_006710362.1:c.174C>G	XP_006710425.1:p.Pro58=
XM_011540707.1:c.444C>G	XP_011539009.1:p.Pro148=
XM_011540708.1:c.444C>G	XP_011539010.1:p.Pro148=
NM_001349881.1:c.444C>G	NP_001336810.1:p.Pro148=
NM_001349882.1:c.444C>G	NP_001336811.1:p.Pro148=
NM_001349884.1:c.444C>G	NP_001336813.1:p.Pro148=
NM_001349885.1:c.444C>G	NP_001336814.1:p.Pro148=
NM_001349886.1:c.174C>G	NP_001336815.1:p.Pro58=
NM_001349887.1:c.174C>G	NP_001336816.1:p.Pro58=
NM_001349888.1:c.174C>G	NP_001336817.1:p.Pro58=
NM_001349889.1:c.54C>G	NP_001336818.1:p.Pro18=
NM_001349890.1:c.54C>G	NP_001336819.1:p.Pro18=
NM_001349891.1:c.54C>G	NP_001336820.1:p.Pro18=
NM_001349892.1:c.54C>G	NP_001336821.1:p.Pro18=
NM_001349893.1:c.54C>G	NP_001336822.1:p.Pro18=
NM_178454.5:c.444C>G	NP_848549.3:p.Pro148=
NR_146301.1:n.701C>G
NR_146302.1:n.561C>G
NR_146303.1:n.912C>G
NR_146304.1:n.772C>G
NR_146305.1:n.755C>G
NR_146306.1:n.727C>G
NR_146307.1:n.800C>G
NR_146308.1:n.867C>G
NM_001349881.2:c.444C>G	NP_001336810.1:p.Pro148=
NM_001349882.2:c.444C>G	NP_001336811.1:p.Pro148=
NM_001349884.2:c.444C>G MANE Select	NP_001336813.1:p.Pro148=
NM_001349885.2:c.444C>G	NP_001336814.1:p.Pro148=
NM_001349886.2:c.174C>G	NP_001336815.1:p.Pro58=
NM_001349887.2:c.174C>G	NP_001336816.1:p.Pro58=
NM_001349888.2:c.174C>G	NP_001336817.1:p.Pro58=
NM_001349889.2:c.54C>G	NP_001336818.1:p.Pro18=
NM_001349890.2:c.54C>G	NP_001336819.1:p.Pro18=
NM_001349891.2:c.54C>G	NP_001336820.1:p.Pro18=
NM_001349892.2:c.54C>G	NP_001336821.1:p.Pro18=
NM_001349893.2:c.54C>G	NP_001336822.1:p.Pro18=
NM_178454.6:c.444C>G	NP_848549.3:p.Pro148=
NR_146301.2:n.578C>G
NR_146302.2:n.438C>G
NR_146303.2:n.789C>G
NR_146304.2:n.649C>G
NR_146305.2:n.632C>G
NR_146306.2:n.604C>G
NR_146307.2:n.677C>G
NR_146308.2:n.744C>G