Canonical Allele Identifier: CA357702814

Gene: DMP1

Linked Data

• MyVariant Identifiers: chr4:g.88584448C>A (hg19) ; chr4:g.87663296C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87663296C>A , CM000666.2:g.87663296C>A	GRCh38
NC_000004.11:g.88584448C>A , CM000666.1:g.88584448C>A	GRCh37
NC_000004.10:g.88803472C>A	NCBI36
NG_008988.1:g.17995C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282479.8:c.1470C>A	ENSP00000282479.6:p.Asp490Glu
ENST00000682752.1:c.*1429C>A	ENSP00000507436.1:n.*1429C>A
ENST00000682781.1:n.1595C>A
ENST00000683764.1:n.1790C>A
ENST00000684240.1:n.1681C>A
ENST00000684389.1:n.1642C>A
ENST00000339673.11:c.1518C>A MANE Select	ENSP00000340935.6:p.Asp506Glu
ENST00000282479.7:c.1470C>A	ENSP00000282479.6:p.Asp490Glu
ENST00000339673.10:c.1518C>A	ENSP00000340935.6:p.Asp506Glu
NM_001079911.2:c.1470C>A	NP_001073380.1:p.Asp490Glu
NM_004407.3:c.1518C>A	NP_004398.1:p.Asp506Glu
XM_011531705.1:c.1605C>A	XP_011530007.1:p.Asp535Glu
XM_011531706.1:c.1557C>A	XP_011530008.1:p.Asp519Glu
XR_938960.1:n.115-5887G>T
XM_011531705.2:c.1605C>A	XP_011530007.1:p.Asp535Glu
XM_011531706.2:c.1557C>A	XP_011530008.1:p.Asp519Glu
XR_938960.2:n.115-5887G>T
NM_001079911.3:c.1470C>A	NP_001073380.1:p.Asp490Glu
NM_004407.4:c.1518C>A MANE Select	NP_004398.1:p.Asp506Glu