Canonical Allele Identifier: CA3002227

Gene: DMP1

Linked Data

• ClinVar Variation Id: 349989
• ClinVar RCV Id: RCV000351172
• dbSNP Id: rs2627724
• ExAC: 4:88584507 G / A
• gnomAD v2: 4-88584507-G-A
• gnomAD v3: 4-87663355-G-A
• gnomAD v4: 4-87663355-G-A
• MyVariant Identifiers: chr4:g.88584507G>A (hg19) ; chr4:g.87663355G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87663355G>A , CM000666.2:g.87663355G>A	GRCh38
NC_000004.11:g.88584507G>A , CM000666.1:g.88584507G>A	GRCh37
NC_000004.10:g.88803531G>A	NCBI36
NG_008988.1:g.18054G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282479.8:c.*35G>A	ENSP00000282479.6:n.*35G>A
ENST00000682752.1:c.*1488G>A	ENSP00000507436.1:n.*1488G>A
ENST00000682781.1:n.1654G>A
ENST00000683764.1:n.1849G>A
ENST00000684240.1:n.1740G>A
ENST00000684389.1:n.1701G>A
ENST00000339673.11:c.*35G>A MANE Select	ENSP00000340935.6:n.*35G>A
ENST00000282479.7:c.*35G>A	ENSP00000282479.6:n.*35G>A
ENST00000339673.10:c.*35G>A	ENSP00000340935.6:n.*35G>A
NM_001079911.2:c.*35G>A	NP_001073380.1:n.*35G>A
NM_004407.3:c.*35G>A	NP_004398.1:n.*35G>A
XM_011531705.1:c.*35G>A	XP_011530007.1:n.*35G>A
XM_011531706.1:c.*35G>A	XP_011530008.1:n.*35G>A
XR_938960.1:n.115-5946C>T
XM_011531705.2:c.*35G>A	XP_011530007.1:n.*35G>A
XM_011531706.2:c.*35G>A	XP_011530008.1:n.*35G>A
XR_938960.2:n.115-5946C>T
NM_001079911.3:c.*35G>A	NP_001073380.1:n.*35G>A
NM_004407.4:c.*35G>A MANE Select	NP_004398.1:n.*35G>A