Canonical Allele Identifier: CA3002166
Gene: DMP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87663008G>A , CM000666.2:g.87663008G>A GRCh38
NC_000004.11:g.88584160G>A , CM000666.1:g.88584160G>A GRCh37
NC_000004.10:g.88803184G>A NCBI36
NG_008988.1:g.17707G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282479.8:c.1182G>A ENSP00000282479.6:p.Glu394=
ENST00000682752.1:c.*1141G>A ENSP00000507436.1:n.*1141G>A
ENST00000682781.1:n.1307G>A
ENST00000683764.1:n.1502G>A
ENST00000684240.1:n.1393G>A
ENST00000684389.1:n.1354G>A
ENST00000339673.11:c.1230G>A MANE Select ENSP00000340935.6:p.Glu410=
ENST00000282479.7:c.1182G>A ENSP00000282479.6:p.Glu394=
ENST00000339673.10:c.1230G>A ENSP00000340935.6:p.Glu410=
NM_001079911.2:c.1182G>A NP_001073380.1:p.Glu394=
NM_004407.3:c.1230G>A NP_004398.1:p.Glu410=
XM_011531705.1:c.1317G>A XP_011530007.1:p.Glu439=
XM_011531706.1:c.1269G>A XP_011530008.1:p.Glu423=
XR_938960.1:n.115-5599C>T
XM_011531705.2:c.1317G>A XP_011530007.1:p.Glu439=
XM_011531706.2:c.1269G>A XP_011530008.1:p.Glu423=
XR_938960.2:n.115-5599C>T
NM_001079911.3:c.1182G>A NP_001073380.1:p.Glu394=
NM_004407.4:c.1230G>A MANE Select NP_004398.1:p.Glu410=