Canonical Allele Identifier: CA357702739

Gene: DMP1

Linked Data

• MyVariant Identifiers: chr4:g.88584429C>G (hg19) ; chr4:g.87663277C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87663277C>G , CM000666.2:g.87663277C>G	GRCh38
NC_000004.11:g.88584429C>G , CM000666.1:g.88584429C>G	GRCh37
NC_000004.10:g.88803453C>G	NCBI36
NG_008988.1:g.17976C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282479.8:c.1451C>G	ENSP00000282479.6:p.Pro484Arg
ENST00000682752.1:c.*1410C>G	ENSP00000507436.1:n.*1410C>G
ENST00000682781.1:n.1576C>G
ENST00000683764.1:n.1771C>G
ENST00000684240.1:n.1662C>G
ENST00000684389.1:n.1623C>G
ENST00000339673.11:c.1499C>G MANE Select	ENSP00000340935.6:p.Pro500Arg
ENST00000282479.7:c.1451C>G	ENSP00000282479.6:p.Pro484Arg
ENST00000339673.10:c.1499C>G	ENSP00000340935.6:p.Pro500Arg
NM_001079911.2:c.1451C>G	NP_001073380.1:p.Pro484Arg
NM_004407.3:c.1499C>G	NP_004398.1:p.Pro500Arg
XM_011531705.1:c.1586C>G	XP_011530007.1:p.Pro529Arg
XM_011531706.1:c.1538C>G	XP_011530008.1:p.Pro513Arg
XR_938960.1:n.115-5868G>C
XM_011531705.2:c.1586C>G	XP_011530007.1:p.Pro529Arg
XM_011531706.2:c.1538C>G	XP_011530008.1:p.Pro513Arg
XR_938960.2:n.115-5868G>C
NM_001079911.3:c.1451C>G	NP_001073380.1:p.Pro484Arg
NM_004407.4:c.1499C>G MANE Select	NP_004398.1:p.Pro500Arg