Canonical Allele Identifier: CA3002016
Gene: DMP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87662126C>T , CM000666.2:g.87662126C>T GRCh38
NC_000004.11:g.88583278C>T , CM000666.1:g.88583278C>T GRCh37
NC_000004.10:g.88802302C>T NCBI36
NG_008988.1:g.16825C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282479.8:c.300C>T ENSP00000282479.6:p.Asp100=
ENST00000682752.1:c.*259C>T ENSP00000507436.1:n.*259C>T
ENST00000682781.1:n.425C>T
ENST00000683764.1:n.620C>T
ENST00000684240.1:n.511C>T
ENST00000684389.1:n.472C>T
ENST00000339673.11:c.348C>T MANE Select ENSP00000340935.6:p.Asp116=
ENST00000282479.7:c.300C>T ENSP00000282479.6:p.Asp100=
ENST00000339673.10:c.348C>T ENSP00000340935.6:p.Asp116=
NM_001079911.2:c.300C>T NP_001073380.1:p.Asp100=
NM_004407.3:c.348C>T NP_004398.1:p.Asp116=
XM_011531705.1:c.435C>T XP_011530007.1:p.Asp145=
XM_011531706.1:c.387C>T XP_011530008.1:p.Asp129=
XR_938960.1:n.115-4717G>A
XM_011531705.2:c.435C>T XP_011530007.1:p.Asp145=
XM_011531706.2:c.387C>T XP_011530008.1:p.Asp129=
XR_938960.2:n.115-4717G>A
NM_001079911.3:c.300C>T NP_001073380.1:p.Asp100=
NM_004407.4:c.348C>T MANE Select NP_004398.1:p.Asp116=