Canonical Allele Identifier: CA357702698
Gene: DMP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87663266T>A , CM000666.2:g.87663266T>A GRCh38
NC_000004.11:g.88584418T>A , CM000666.1:g.88584418T>A GRCh37
NC_000004.10:g.88803442T>A NCBI36
NG_008988.1:g.17965T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282479.8:c.1440T>A ENSP00000282479.6:p.Tyr480Ter
ENST00000682752.1:c.*1399T>A ENSP00000507436.1:n.*1399T>A
ENST00000682781.1:n.1565T>A
ENST00000683764.1:n.1760T>A
ENST00000684240.1:n.1651T>A
ENST00000684389.1:n.1612T>A
ENST00000339673.11:c.1488T>A MANE Select ENSP00000340935.6:p.Tyr496Ter
ENST00000282479.7:c.1440T>A ENSP00000282479.6:p.Tyr480Ter
ENST00000339673.10:c.1488T>A ENSP00000340935.6:p.Tyr496Ter
NM_001079911.2:c.1440T>A NP_001073380.1:p.Tyr480Ter
NM_004407.3:c.1488T>A NP_004398.1:p.Tyr496Ter
XM_011531705.1:c.1575T>A XP_011530007.1:p.Tyr525Ter
XM_011531706.1:c.1527T>A XP_011530008.1:p.Tyr509Ter
XR_938960.1:n.115-5857A>T
XM_011531705.2:c.1575T>A XP_011530007.1:p.Tyr525Ter
XM_011531706.2:c.1527T>A XP_011530008.1:p.Tyr509Ter
XR_938960.2:n.115-5857A>T
NM_001079911.3:c.1440T>A NP_001073380.1:p.Tyr480Ter
NM_004407.4:c.1488T>A MANE Select NP_004398.1:p.Tyr496Ter