Canonical Allele Identifier: CA357702836

Gene: DMP1

Linked Data

• MyVariant Identifiers: chr4:g.88584453A>T (hg19) ; chr4:g.87663301A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87663301A>T , CM000666.2:g.87663301A>T	GRCh38
NC_000004.11:g.88584453A>T , CM000666.1:g.88584453A>T	GRCh37
NC_000004.10:g.88803477A>T	NCBI36
NG_008988.1:g.18000A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282479.8:c.1475A>T	ENSP00000282479.6:p.Asp492Val
ENST00000682752.1:c.*1434A>T	ENSP00000507436.1:n.*1434A>T
ENST00000682781.1:n.1600A>T
ENST00000683764.1:n.1795A>T
ENST00000684240.1:n.1686A>T
ENST00000684389.1:n.1647A>T
ENST00000339673.11:c.1523A>T MANE Select	ENSP00000340935.6:p.Asp508Val
ENST00000282479.7:c.1475A>T	ENSP00000282479.6:p.Asp492Val
ENST00000339673.10:c.1523A>T	ENSP00000340935.6:p.Asp508Val
NM_001079911.2:c.1475A>T	NP_001073380.1:p.Asp492Val
NM_004407.3:c.1523A>T	NP_004398.1:p.Asp508Val
XM_011531705.1:c.1610A>T	XP_011530007.1:p.Asp537Val
XM_011531706.1:c.1562A>T	XP_011530008.1:p.Asp521Val
XR_938960.1:n.115-5892T>A
XM_011531705.2:c.1610A>T	XP_011530007.1:p.Asp537Val
XM_011531706.2:c.1562A>T	XP_011530008.1:p.Asp521Val
XR_938960.2:n.115-5892T>A
NM_001079911.3:c.1475A>T	NP_001073380.1:p.Asp492Val
NM_004407.4:c.1523A>T MANE Select	NP_004398.1:p.Asp508Val