Canonical Allele Identifier: CA2671360925
Gene: DMP1 HGNC NCBI

Linked Data

gnomAD v4: 4-87661886-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87661886A>C , CM000666.2:g.87661886A>C GRCh38
NC_000004.11:g.88583038A>C , CM000666.1:g.88583038A>C GRCh37
NC_000004.10:g.88802062A>C NCBI36
NG_008988.1:g.16585A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000282479.8:c.136-76A>C ENSP00000282479.6:n.136-76A>C
ENST00000682752.1:c.*95-76A>C ENSP00000507436.1:n.*95-76A>C
ENST00000682781.1:n.261-76A>C
ENST00000683764.1:n.456-76A>C
ENST00000684240.1:n.347-76A>C
ENST00000684389.1:n.308-76A>C
ENST00000339673.11:c.184-76A>C MANE Select ENSP00000340935.6:n.184-76A>C
ENST00000282479.7:c.136-76A>C ENSP00000282479.6:n.136-76A>C
ENST00000339673.10:c.184-76A>C ENSP00000340935.6:n.184-76A>C
NM_001079911.2:c.136-76A>C NP_001073380.1:n.136-76A>C
NM_004407.3:c.184-76A>C NP_004398.1:n.184-76A>C
XM_011531705.1:c.271-76A>C XP_011530007.1:n.271-76A>C
XM_011531706.1:c.223-76A>C XP_011530008.1:n.223-76A>C
XR_938960.1:n.115-4477T>G
XM_011531705.2:c.271-76A>C XP_011530007.1:n.271-76A>C
XM_011531706.2:c.223-76A>C XP_011530008.1:n.223-76A>C
XR_938960.2:n.115-4477T>G
NM_001079911.3:c.136-76A>C NP_001073380.1:n.136-76A>C
NM_004407.4:c.184-76A>C MANE Select NP_004398.1:n.184-76A>C