Canonical Allele Identifier: CA440287951
Gene: DMP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.88584427A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87663275A>G , CM000666.2:g.87663275A>G GRCh38
NC_000004.11:g.88584427A>G , CM000666.1:g.88584427A>G GRCh37
NC_000004.10:g.88803451A>G NCBI36
NG_008988.1:g.17974A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282479.8:c.1449A>G ENSP00000282479.6:p.Lys483=
ENST00000682752.1:c.*1408A>G ENSP00000507436.1:n.*1408A>G
ENST00000682781.1:n.1574A>G
ENST00000683764.1:n.1769A>G
ENST00000684240.1:n.1660A>G
ENST00000684389.1:n.1621A>G
ENST00000339673.11:c.1497A>G MANE Select ENSP00000340935.6:p.Lys499=
ENST00000282479.7:c.1449A>G ENSP00000282479.6:p.Lys483=
ENST00000339673.10:c.1497A>G ENSP00000340935.6:p.Lys499=
NM_001079911.2:c.1449A>G NP_001073380.1:p.Lys483=
NM_004407.3:c.1497A>G NP_004398.1:p.Lys499=
XM_011531705.1:c.1584A>G XP_011530007.1:p.Lys528=
XM_011531706.1:c.1536A>G XP_011530008.1:p.Lys512=
XR_938960.1:n.115-5866T>C
XM_011531705.2:c.1584A>G XP_011530007.1:p.Lys528=
XM_011531706.2:c.1536A>G XP_011530008.1:p.Lys512=
XR_938960.2:n.115-5866T>C
NM_001079911.3:c.1449A>G NP_001073380.1:p.Lys483=
NM_004407.4:c.1497A>G MANE Select NP_004398.1:p.Lys499=