Canonical Allele Identifier: CA1474407302
Gene: DMP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87663271A= , CM000666.2:g.87663271A= GRCh38
NC_000004.11:g.88584423A= , CM000666.1:g.88584423A= GRCh37
NC_000004.10:g.88803447A= NCBI36
NG_008988.1:g.17970A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282479.8:c.1445A= ENSP00000282479.6:p.Asn482=
ENST00000682752.1:c.*1404A= ENSP00000507436.1:n.*1404A=
ENST00000682781.1:n.1570A=
ENST00000683764.1:n.1765A=
ENST00000684240.1:n.1656A=
ENST00000684389.1:n.1617A=
ENST00000339673.11:c.1493A= MANE Select ENSP00000340935.6:p.Asn498=
ENST00000282479.7:c.1445A= ENSP00000282479.6:p.Asn482=
ENST00000339673.10:c.1493A= ENSP00000340935.6:p.Asn498=
NM_001079911.2:c.1445A= NP_001073380.1:p.Asn482=
NM_004407.3:c.1493A= NP_004398.1:p.Asn498=
XM_011531705.1:c.1580A= XP_011530007.1:p.Asn527=
XM_011531706.1:c.1532A= XP_011530008.1:p.Asn511=
XR_938960.1:n.115-5862T=
XM_011531705.2:c.1580A= XP_011530007.1:p.Asn527=
XM_011531706.2:c.1532A= XP_011530008.1:p.Asn511=
XR_938960.2:n.115-5862T=
NM_001079911.3:c.1445A= NP_001073380.1:p.Asn482=
NM_004407.4:c.1493A= MANE Select NP_004398.1:p.Asn498=