Canonical Allele Identifier: CA341818897

Gene: DRAM2

Linked Data

• MyVariant Identifiers: chr1:g.111663214C>A (hg19) ; chr1:g.111120592C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111120592C>A , CM000663.2:g.111120592C>A	GRCh38
NC_000001.10:g.111663214C>A , CM000663.1:g.111663214C>A	GRCh37
NC_000001.9:g.111464737C>A	NCBI36
NG_053089.1:g.24625G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484310.6:c.441G>T MANE Select	ENSP00000503400.1:p.Gln147His
ENST00000539140.6:c.441G>T	ENSP00000437718.1:p.Gln147His
ENST00000286692.8:c.441G>T	ENSP00000286692.4:p.Gln147His
ENST00000461449.5:n.215G>T
ENST00000462092.5:n.762G>T
ENST00000477588.5:n.5G>T
ENST00000477769.1:n.9G>T
ENST00000480600.6:n.457G>T
ENST00000484310.5:n.685G>T
ENST00000496430.6:c.*128G>T	ENSP00000473779.1:n.*128G>T
ENST00000539140.5:c.441G>T	ENSP00000437718.1:p.Gln147His
NM_178454.4:c.441G>T	NP_848549.3:p.Gln147His
XM_005270469.1:c.441G>T	XP_005270526.1:p.Gln147His
XM_005270470.1:c.441G>T	XP_005270527.1:p.Gln147His
XM_006710361.1:c.171G>T	XP_006710424.1:p.Gln57His
XM_006710362.1:c.171G>T	XP_006710425.1:p.Gln57His
XM_011540707.1:c.441G>T	XP_011539009.1:p.Gln147His
XM_011540708.1:c.441G>T	XP_011539010.1:p.Gln147His
NM_001349881.1:c.441G>T	NP_001336810.1:p.Gln147His
NM_001349882.1:c.441G>T	NP_001336811.1:p.Gln147His
NM_001349884.1:c.441G>T	NP_001336813.1:p.Gln147His
NM_001349885.1:c.441G>T	NP_001336814.1:p.Gln147His
NM_001349886.1:c.171G>T	NP_001336815.1:p.Gln57His
NM_001349887.1:c.171G>T	NP_001336816.1:p.Gln57His
NM_001349888.1:c.171G>T	NP_001336817.1:p.Gln57His
NM_001349889.1:c.51G>T	NP_001336818.1:p.Gln17His
NM_001349890.1:c.51G>T	NP_001336819.1:p.Gln17His
NM_001349891.1:c.51G>T	NP_001336820.1:p.Gln17His
NM_001349892.1:c.51G>T	NP_001336821.1:p.Gln17His
NM_001349893.1:c.51G>T	NP_001336822.1:p.Gln17His
NM_178454.5:c.441G>T	NP_848549.3:p.Gln147His
NR_146301.1:n.698G>T
NR_146302.1:n.558G>T
NR_146303.1:n.909G>T
NR_146304.1:n.769G>T
NR_146305.1:n.752G>T
NR_146306.1:n.724G>T
NR_146307.1:n.797G>T
NR_146308.1:n.864G>T
NM_001349881.2:c.441G>T	NP_001336810.1:p.Gln147His
NM_001349882.2:c.441G>T	NP_001336811.1:p.Gln147His
NM_001349884.2:c.441G>T MANE Select	NP_001336813.1:p.Gln147His
NM_001349885.2:c.441G>T	NP_001336814.1:p.Gln147His
NM_001349886.2:c.171G>T	NP_001336815.1:p.Gln57His
NM_001349887.2:c.171G>T	NP_001336816.1:p.Gln57His
NM_001349888.2:c.171G>T	NP_001336817.1:p.Gln57His
NM_001349889.2:c.51G>T	NP_001336818.1:p.Gln17His
NM_001349890.2:c.51G>T	NP_001336819.1:p.Gln17His
NM_001349891.2:c.51G>T	NP_001336820.1:p.Gln17His
NM_001349892.2:c.51G>T	NP_001336821.1:p.Gln17His
NM_001349893.2:c.51G>T	NP_001336822.1:p.Gln17His
NM_178454.6:c.441G>T	NP_848549.3:p.Gln147His
NR_146301.2:n.575G>T
NR_146302.2:n.435G>T
NR_146303.2:n.786G>T
NR_146304.2:n.646G>T
NR_146305.2:n.629G>T
NR_146306.2:n.601G>T
NR_146307.2:n.674G>T
NR_146308.2:n.741G>T