Canonical Allele Identifier: CA440287969
Gene: DMP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.88584466C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87663314C>G , CM000666.2:g.87663314C>G GRCh38
NC_000004.11:g.88584466C>G , CM000666.1:g.88584466C>G GRCh37
NC_000004.10:g.88803490C>G NCBI36
NG_008988.1:g.18013C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282479.8:c.1488C>G ENSP00000282479.6:p.Gly496=
ENST00000682752.1:c.*1447C>G ENSP00000507436.1:n.*1447C>G
ENST00000682781.1:n.1613C>G
ENST00000683764.1:n.1808C>G
ENST00000684240.1:n.1699C>G
ENST00000684389.1:n.1660C>G
ENST00000339673.11:c.1536C>G MANE Select ENSP00000340935.6:p.Gly512=
ENST00000282479.7:c.1488C>G ENSP00000282479.6:p.Gly496=
ENST00000339673.10:c.1536C>G ENSP00000340935.6:p.Gly512=
NM_001079911.2:c.1488C>G NP_001073380.1:p.Gly496=
NM_004407.3:c.1536C>G NP_004398.1:p.Gly512=
XM_011531705.1:c.1623C>G XP_011530007.1:p.Gly541=
XM_011531706.1:c.1575C>G XP_011530008.1:p.Gly525=
XR_938960.1:n.115-5905G>C
XM_011531705.2:c.1623C>G XP_011530007.1:p.Gly541=
XM_011531706.2:c.1575C>G XP_011530008.1:p.Gly525=
XR_938960.2:n.115-5905G>C
NM_001079911.3:c.1488C>G NP_001073380.1:p.Gly496=
NM_004407.4:c.1536C>G MANE Select NP_004398.1:p.Gly512=