Canonical Allele Identifier: CA553087509

Gene: DMP1

Linked Data

• dbSNP Id: rs1236917900
• gnomAD v2: 4-88583061-C-A
• gnomAD v3: 4-87661909-C-A
• gnomAD v4: 4-87661909-C-A
• MyVariant Identifiers: chr4:g.88583061C>A (hg19) ; chr4:g.87661909C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87661909C>A , CM000666.2:g.87661909C>A	GRCh38
NC_000004.11:g.88583061C>A , CM000666.1:g.88583061C>A	GRCh37
NC_000004.10:g.88802085C>A	NCBI36
NG_008988.1:g.16608C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000282479.8:c.136-53C>A	ENSP00000282479.6:n.136-53C>A
ENST00000682752.1:c.*95-53C>A	ENSP00000507436.1:n.*95-53C>A
ENST00000682781.1:n.261-53C>A
ENST00000683764.1:n.456-53C>A
ENST00000684240.1:n.347-53C>A
ENST00000684389.1:n.308-53C>A
ENST00000339673.11:c.184-53C>A MANE Select	ENSP00000340935.6:n.184-53C>A
ENST00000282479.7:c.136-53C>A	ENSP00000282479.6:n.136-53C>A
ENST00000339673.10:c.184-53C>A	ENSP00000340935.6:n.184-53C>A
NM_001079911.2:c.136-53C>A	NP_001073380.1:n.136-53C>A
NM_004407.3:c.184-53C>A	NP_004398.1:n.184-53C>A
XM_011531705.1:c.271-53C>A	XP_011530007.1:n.271-53C>A
XM_011531706.1:c.223-53C>A	XP_011530008.1:n.223-53C>A
XR_938960.1:n.115-4500G>T
XM_011531705.2:c.271-53C>A	XP_011530007.1:n.271-53C>A
XM_011531706.2:c.223-53C>A	XP_011530008.1:n.223-53C>A
XR_938960.2:n.115-4500G>T
NM_001079911.3:c.136-53C>A	NP_001073380.1:n.136-53C>A
NM_004407.4:c.184-53C>A MANE Select	NP_004398.1:n.184-53C>A