Canonical Allele Identifier: CA799555751

Gene: DMP1

Linked Data

• dbSNP Id: rs1365510050
• gnomAD v4: 4-87663365-G-A
• MyVariant Identifiers: chr4:g.88584517G>A (hg19) ; chr4:g.87663365G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87663365G>A , CM000666.2:g.87663365G>A	GRCh38
NC_000004.11:g.88584517G>A , CM000666.1:g.88584517G>A	GRCh37
NC_000004.10:g.88803541G>A	NCBI36
NG_008988.1:g.18064G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282479.8:c.*45G>A	ENSP00000282479.6:n.*45G>A
ENST00000682752.1:c.*1498G>A	ENSP00000507436.1:n.*1498G>A
ENST00000682781.1:n.1664G>A
ENST00000683764.1:n.1859G>A
ENST00000684240.1:n.1750G>A
ENST00000684389.1:n.1711G>A
ENST00000339673.11:c.*45G>A MANE Select	ENSP00000340935.6:n.*45G>A
ENST00000282479.7:c.*45G>A	ENSP00000282479.6:n.*45G>A
ENST00000339673.10:c.*45G>A	ENSP00000340935.6:n.*45G>A
NM_001079911.2:c.*45G>A	NP_001073380.1:n.*45G>A
NM_004407.3:c.*45G>A	NP_004398.1:n.*45G>A
XM_011531705.1:c.*45G>A	XP_011530007.1:n.*45G>A
XM_011531706.1:c.*45G>A	XP_011530008.1:n.*45G>A
XR_938960.1:n.115-5956C>T
XM_011531705.2:c.*45G>A	XP_011530007.1:n.*45G>A
XM_011531706.2:c.*45G>A	XP_011530008.1:n.*45G>A
XR_938960.2:n.115-5956C>T
NM_001079911.3:c.*45G>A	NP_001073380.1:n.*45G>A
NM_004407.4:c.*45G>A MANE Select	NP_004398.1:n.*45G>A