Canonical Allele Identifier: CA200119
Gene: DRAM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 192237
dbSNP Id: rs786205664

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111120671T>A , CM000663.2:g.111120671T>A GRCh38
NC_000001.10:g.111663293T>A , CM000663.1:g.111663293T>A GRCh37
NC_000001.9:g.111464816T>A NCBI36
NG_053089.1:g.24546A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000484310.6:c.362A>T MANE Select ENSP00000503400.1:p.His121Leu
ENST00000539140.6:c.362A>T ENSP00000437718.1:p.His121Leu
ENST00000286692.8:c.362A>T ENSP00000286692.4:p.His121Leu
ENST00000461449.5:n.136A>T
ENST00000462092.5:n.683A>T
ENST00000480600.6:n.378A>T
ENST00000484310.5:n.606A>T
ENST00000496430.6:c.*49A>T ENSP00000473779.1:n.*49A>T
ENST00000539140.5:c.362A>T ENSP00000437718.1:p.His121Leu
NM_178454.4:c.362A>T NP_848549.3:p.His121Leu
XM_005270469.1:c.362A>T XP_005270526.1:p.His121Leu
XM_005270470.1:c.362A>T XP_005270527.1:p.His121Leu
XM_006710361.1:c.92A>T XP_006710424.1:p.His31Leu
XM_006710362.1:c.92A>T XP_006710425.1:p.His31Leu
XM_011540707.1:c.362A>T XP_011539009.1:p.His121Leu
XM_011540708.1:c.362A>T XP_011539010.1:p.His121Leu
NM_001349881.1:c.362A>T NP_001336810.1:p.His121Leu
NM_001349882.1:c.362A>T NP_001336811.1:p.His121Leu
NM_001349884.1:c.362A>T NP_001336813.1:p.His121Leu
NM_001349885.1:c.362A>T NP_001336814.1:p.His121Leu
NM_001349886.1:c.92A>T NP_001336815.1:p.His31Leu
NM_001349887.1:c.92A>T NP_001336816.1:p.His31Leu
NM_001349888.1:c.92A>T NP_001336817.1:p.His31Leu
NM_001349889.1:c.-29A>T NP_001336818.1:n.-29A>T
NM_001349890.1:c.-29A>T NP_001336819.1:n.-29A>T
NM_001349891.1:c.-29A>T NP_001336820.1:n.-29A>T
NM_001349892.1:c.-29A>T NP_001336821.1:n.-29A>T
NM_001349893.1:c.-29A>T NP_001336822.1:n.-29A>T
NM_178454.5:c.362A>T NP_848549.3:p.His121Leu
NR_146301.1:n.619A>T
NR_146302.1:n.479A>T
NR_146303.1:n.830A>T
NR_146304.1:n.690A>T
NR_146305.1:n.673A>T
NR_146306.1:n.645A>T
NR_146307.1:n.718A>T
NR_146308.1:n.785A>T
NM_001349881.2:c.362A>T NP_001336810.1:p.His121Leu
NM_001349882.2:c.362A>T NP_001336811.1:p.His121Leu
NM_001349884.2:c.362A>T MANE Select NP_001336813.1:p.His121Leu
NM_001349885.2:c.362A>T NP_001336814.1:p.His121Leu
NM_001349886.2:c.92A>T NP_001336815.1:p.His31Leu
NM_001349887.2:c.92A>T NP_001336816.1:p.His31Leu
NM_001349888.2:c.92A>T NP_001336817.1:p.His31Leu
NM_001349889.2:c.-29A>T NP_001336818.1:n.-29A>T
NM_001349890.2:c.-29A>T NP_001336819.1:n.-29A>T
NM_001349891.2:c.-29A>T NP_001336820.1:n.-29A>T
NM_001349892.2:c.-29A>T NP_001336821.1:n.-29A>T
NM_001349893.2:c.-29A>T NP_001336822.1:n.-29A>T
NM_178454.6:c.362A>T NP_848549.3:p.His121Leu
NR_146301.2:n.496A>T
NR_146302.2:n.356A>T
NR_146303.2:n.707A>T
NR_146304.2:n.567A>T
NR_146305.2:n.550A>T
NR_146306.2:n.522A>T
NR_146307.2:n.595A>T
NR_146308.2:n.662A>T