Canonical Allele Identifier: CA341818940

Gene: DRAM2

Linked Data

• MyVariant Identifiers: chr1:g.111663233A>C (hg19) ; chr1:g.111120611A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111120611A>C , CM000663.2:g.111120611A>C	GRCh38
NC_000001.10:g.111663233A>C , CM000663.1:g.111663233A>C	GRCh37
NC_000001.9:g.111464756A>C	NCBI36
NG_053089.1:g.24606T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484310.6:c.422T>G MANE Select	ENSP00000503400.1:p.Ile141Ser
ENST00000539140.6:c.422T>G	ENSP00000437718.1:p.Ile141Ser
ENST00000286692.8:c.422T>G	ENSP00000286692.4:p.Ile141Ser
ENST00000461449.5:n.196T>G
ENST00000462092.5:n.743T>G
ENST00000480600.6:n.438T>G
ENST00000484310.5:n.666T>G
ENST00000496430.6:c.*109T>G	ENSP00000473779.1:n.*109T>G
ENST00000539140.5:c.422T>G	ENSP00000437718.1:p.Ile141Ser
NM_178454.4:c.422T>G	NP_848549.3:p.Ile141Ser
XM_005270469.1:c.422T>G	XP_005270526.1:p.Ile141Ser
XM_005270470.1:c.422T>G	XP_005270527.1:p.Ile141Ser
XM_006710361.1:c.152T>G	XP_006710424.1:p.Ile51Ser
XM_006710362.1:c.152T>G	XP_006710425.1:p.Ile51Ser
XM_011540707.1:c.422T>G	XP_011539009.1:p.Ile141Ser
XM_011540708.1:c.422T>G	XP_011539010.1:p.Ile141Ser
NM_001349881.1:c.422T>G	NP_001336810.1:p.Ile141Ser
NM_001349882.1:c.422T>G	NP_001336811.1:p.Ile141Ser
NM_001349884.1:c.422T>G	NP_001336813.1:p.Ile141Ser
NM_001349885.1:c.422T>G	NP_001336814.1:p.Ile141Ser
NM_001349886.1:c.152T>G	NP_001336815.1:p.Ile51Ser
NM_001349887.1:c.152T>G	NP_001336816.1:p.Ile51Ser
NM_001349888.1:c.152T>G	NP_001336817.1:p.Ile51Ser
NM_001349889.1:c.32T>G	NP_001336818.1:p.Ile11Ser
NM_001349890.1:c.32T>G	NP_001336819.1:p.Ile11Ser
NM_001349891.1:c.32T>G	NP_001336820.1:p.Ile11Ser
NM_001349892.1:c.32T>G	NP_001336821.1:p.Ile11Ser
NM_001349893.1:c.32T>G	NP_001336822.1:p.Ile11Ser
NM_178454.5:c.422T>G	NP_848549.3:p.Ile141Ser
NR_146301.1:n.679T>G
NR_146302.1:n.539T>G
NR_146303.1:n.890T>G
NR_146304.1:n.750T>G
NR_146305.1:n.733T>G
NR_146306.1:n.705T>G
NR_146307.1:n.778T>G
NR_146308.1:n.845T>G
NM_001349881.2:c.422T>G	NP_001336810.1:p.Ile141Ser
NM_001349882.2:c.422T>G	NP_001336811.1:p.Ile141Ser
NM_001349884.2:c.422T>G MANE Select	NP_001336813.1:p.Ile141Ser
NM_001349885.2:c.422T>G	NP_001336814.1:p.Ile141Ser
NM_001349886.2:c.152T>G	NP_001336815.1:p.Ile51Ser
NM_001349887.2:c.152T>G	NP_001336816.1:p.Ile51Ser
NM_001349888.2:c.152T>G	NP_001336817.1:p.Ile51Ser
NM_001349889.2:c.32T>G	NP_001336818.1:p.Ile11Ser
NM_001349890.2:c.32T>G	NP_001336819.1:p.Ile11Ser
NM_001349891.2:c.32T>G	NP_001336820.1:p.Ile11Ser
NM_001349892.2:c.32T>G	NP_001336821.1:p.Ile11Ser
NM_001349893.2:c.32T>G	NP_001336822.1:p.Ile11Ser
NM_178454.6:c.422T>G	NP_848549.3:p.Ile141Ser
NR_146301.2:n.556T>G
NR_146302.2:n.416T>G
NR_146303.2:n.767T>G
NR_146304.2:n.627T>G
NR_146305.2:n.610T>G
NR_146306.2:n.582T>G
NR_146307.2:n.655T>G
NR_146308.2:n.722T>G