Canonical Allele Identifier: CA101381260

Gene: DMP1

Linked Data

• dbSNP Id: rs543756426
• gnomAD v2: 4-88577492-C-A
• gnomAD v3: 4-87656340-C-A
• gnomAD v4: 4-87656340-C-A
• MyVariant Identifiers: chr4:g.88577492C>A (hg19) ; chr4:g.87656340C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87656340C>A , CM000666.2:g.87656340C>A	GRCh38
NC_000004.11:g.88577492C>A , CM000666.1:g.88577492C>A	GRCh37
NC_000004.10:g.88796516C>A	NCBI36
NG_008988.1:g.11039C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282479.8:c.-21-132C>A	ENSP00000282479.6:n.-21-132C>A
ENST00000682752.1:c.-21-132C>A	ENSP00000507436.1:n.-21-132C>A
ENST00000682781.1:n.105-132C>A
ENST00000683764.1:n.143-132C>A
ENST00000684240.1:n.143-132C>A
ENST00000684389.1:n.104-132C>A
ENST00000339673.11:c.-21-132C>A MANE Select	ENSP00000340935.6:n.-21-132C>A
ENST00000282479.7:c.-21-132C>A	ENSP00000282479.6:n.-21-132C>A
ENST00000339673.10:c.-21-132C>A	ENSP00000340935.6:n.-21-132C>A
NM_001079911.2:c.-21-132C>A	NP_001073380.1:n.-21-132C>A
NM_004407.3:c.-21-132C>A	NP_004398.1:n.-21-132C>A
XM_011531705.1:c.67-132C>A	XP_011530007.1:n.67-132C>A
XM_011531706.1:c.67-132C>A	XP_011530008.1:n.67-132C>A
XM_011531705.2:c.67-132C>A	XP_011530007.1:n.67-132C>A
XM_011531706.2:c.67-132C>A	XP_011530008.1:n.67-132C>A
NM_001079911.3:c.-21-132C>A	NP_001073380.1:n.-21-132C>A
NM_004407.4:c.-21-132C>A MANE Select	NP_004398.1:n.-21-132C>A