Canonical Allele Identifier: CA1474404290
Gene: DMP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87656315T= , CM000666.2:g.87656315T= GRCh38
NC_000004.11:g.88577467T= , CM000666.1:g.88577467T= GRCh37
NC_000004.10:g.88796491T= NCBI36
NG_008988.1:g.11014T=

Transcript Alleles

HGVS Amino-acid change
ENST00000282479.8:c.-21-157T= ENSP00000282479.6:n.-21-157T=
ENST00000682752.1:c.-21-157T= ENSP00000507436.1:n.-21-157T=
ENST00000682781.1:n.105-157T=
ENST00000683764.1:n.143-157T=
ENST00000684240.1:n.143-157T=
ENST00000684389.1:n.104-157T=
ENST00000339673.11:c.-21-157T= MANE Select ENSP00000340935.6:n.-21-157T=
ENST00000282479.7:c.-21-157T= ENSP00000282479.6:n.-21-157T=
ENST00000339673.10:c.-21-157T= ENSP00000340935.6:n.-21-157T=
NM_001079911.2:c.-21-157T= NP_001073380.1:n.-21-157T=
NM_004407.3:c.-21-157T= NP_004398.1:n.-21-157T=
XM_011531705.1:c.67-157T= XP_011530007.1:n.67-157T=
XM_011531706.1:c.67-157T= XP_011530008.1:n.67-157T=
XM_011531705.2:c.67-157T= XP_011530007.1:n.67-157T=
XM_011531706.2:c.67-157T= XP_011530008.1:n.67-157T=
NM_001079911.3:c.-21-157T= NP_001073380.1:n.-21-157T=
NM_004407.4:c.-21-157T= MANE Select NP_004398.1:n.-21-157T=