Canonical Allele Identifier: CA3002216
Gene: DMP1 HGNC NCBI

Linked Data

dbSNP Id: rs756030027
gnomAD v2: 4-88584451-T-A
gnomAD v4: 4-87663299-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87663299T>A , CM000666.2:g.87663299T>A GRCh38
NC_000004.11:g.88584451T>A , CM000666.1:g.88584451T>A GRCh37
NC_000004.10:g.88803475T>A NCBI36
NG_008988.1:g.17998T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282479.8:c.1473T>A ENSP00000282479.6:p.Asn491Lys
ENST00000682752.1:c.*1432T>A ENSP00000507436.1:n.*1432T>A
ENST00000682781.1:n.1598T>A
ENST00000683764.1:n.1793T>A
ENST00000684240.1:n.1684T>A
ENST00000684389.1:n.1645T>A
ENST00000339673.11:c.1521T>A MANE Select ENSP00000340935.6:p.Asn507Lys
ENST00000282479.7:c.1473T>A ENSP00000282479.6:p.Asn491Lys
ENST00000339673.10:c.1521T>A ENSP00000340935.6:p.Asn507Lys
NM_001079911.2:c.1473T>A NP_001073380.1:p.Asn491Lys
NM_004407.3:c.1521T>A NP_004398.1:p.Asn507Lys
XM_011531705.1:c.1608T>A XP_011530007.1:p.Asn536Lys
XM_011531706.1:c.1560T>A XP_011530008.1:p.Asn520Lys
XR_938960.1:n.115-5890A>T
XM_011531705.2:c.1608T>A XP_011530007.1:p.Asn536Lys
XM_011531706.2:c.1560T>A XP_011530008.1:p.Asn520Lys
XR_938960.2:n.115-5890A>T
NM_001079911.3:c.1473T>A NP_001073380.1:p.Asn491Lys
NM_004407.4:c.1521T>A MANE Select NP_004398.1:p.Asn507Lys