Canonical Allele Identifier: CA1474406733
Gene: DMP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87661914C= , CM000666.2:g.87661914C= GRCh38
NC_000004.11:g.88583066C= , CM000666.1:g.88583066C= GRCh37
NC_000004.10:g.88802090C= NCBI36
NG_008988.1:g.16613C=

Transcript Alleles

HGVS Amino-acid change
ENST00000282479.8:c.136-48C= ENSP00000282479.6:n.136-48C=
ENST00000682752.1:c.*95-48C= ENSP00000507436.1:n.*95-48C=
ENST00000682781.1:n.261-48C=
ENST00000683764.1:n.456-48C=
ENST00000684240.1:n.347-48C=
ENST00000684389.1:n.308-48C=
ENST00000339673.11:c.184-48C= MANE Select ENSP00000340935.6:n.184-48C=
ENST00000282479.7:c.136-48C= ENSP00000282479.6:n.136-48C=
ENST00000339673.10:c.184-48C= ENSP00000340935.6:n.184-48C=
NM_001079911.2:c.136-48C= NP_001073380.1:n.136-48C=
NM_004407.3:c.184-48C= NP_004398.1:n.184-48C=
XM_011531705.1:c.271-48C= XP_011530007.1:n.271-48C=
XM_011531706.1:c.223-48C= XP_011530008.1:n.223-48C=
XR_938960.1:n.115-4505G=
XM_011531705.2:c.271-48C= XP_011530007.1:n.271-48C=
XM_011531706.2:c.223-48C= XP_011530008.1:n.223-48C=
XR_938960.2:n.115-4505G=
NM_001079911.3:c.136-48C= NP_001073380.1:n.136-48C=
NM_004407.4:c.184-48C= MANE Select NP_004398.1:n.184-48C=