Canonical Allele Identifier: CA1474404376
Gene: DMP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87656501C= , CM000666.2:g.87656501C= GRCh38
NC_000004.11:g.88577653C= , CM000666.1:g.88577653C= GRCh37
NC_000004.10:g.88796677C= NCBI36
NG_008988.1:g.11200C=

Transcript Alleles

HGVS Amino-acid change
ENST00000282479.8:c.9C= ENSP00000282479.6:p.Ile3=
ENST00000682752.1:c.9C= ENSP00000507436.1:p.Ile3=
ENST00000682781.1:n.134C=
ENST00000683764.1:n.172C=
ENST00000684240.1:n.172C=
ENST00000684389.1:n.133C=
ENST00000339673.11:c.9C= MANE Select ENSP00000340935.6:p.Ile3=
ENST00000282479.7:c.9C= ENSP00000282479.6:p.Ile3=
ENST00000339673.10:c.9C= ENSP00000340935.6:p.Ile3=
NM_001079911.2:c.9C= NP_001073380.1:p.Ile3=
NM_004407.3:c.9C= NP_004398.1:p.Ile3=
XM_011531705.1:c.96C= XP_011530007.1:p.Ile32=
XM_011531706.1:c.96C= XP_011530008.1:p.Ile32=
XM_011531705.2:c.96C= XP_011530007.1:p.Ile32=
XM_011531706.2:c.96C= XP_011530008.1:p.Ile32=
NM_001079911.3:c.9C= NP_001073380.1:p.Ile3=
NM_004407.4:c.9C= MANE Select NP_004398.1:p.Ile3=