Canonical Allele Identifier: CA2671360936

Gene: DMP1

Linked Data

• gnomAD v4: 4-87661910-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87661910T>A , CM000666.2:g.87661910T>A	GRCh38
NC_000004.11:g.88583062T>A , CM000666.1:g.88583062T>A	GRCh37
NC_000004.10:g.88802086T>A	NCBI36
NG_008988.1:g.16609T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000282479.8:c.136-52T>A	ENSP00000282479.6:n.136-52T>A
ENST00000682752.1:c.*95-52T>A	ENSP00000507436.1:n.*95-52T>A
ENST00000682781.1:n.261-52T>A
ENST00000683764.1:n.456-52T>A
ENST00000684240.1:n.347-52T>A
ENST00000684389.1:n.308-52T>A
ENST00000339673.11:c.184-52T>A MANE Select	ENSP00000340935.6:n.184-52T>A
ENST00000282479.7:c.136-52T>A	ENSP00000282479.6:n.136-52T>A
ENST00000339673.10:c.184-52T>A	ENSP00000340935.6:n.184-52T>A
NM_001079911.2:c.136-52T>A	NP_001073380.1:n.136-52T>A
NM_004407.3:c.184-52T>A	NP_004398.1:n.184-52T>A
XM_011531705.1:c.271-52T>A	XP_011530007.1:n.271-52T>A
XM_011531706.1:c.223-52T>A	XP_011530008.1:n.223-52T>A
XR_938960.1:n.115-4501A>T
XM_011531705.2:c.271-52T>A	XP_011530007.1:n.271-52T>A
XM_011531706.2:c.223-52T>A	XP_011530008.1:n.223-52T>A
XR_938960.2:n.115-4501A>T
NM_001079911.3:c.136-52T>A	NP_001073380.1:n.136-52T>A
NM_004407.4:c.184-52T>A MANE Select	NP_004398.1:n.184-52T>A