Canonical Allele Identifier: CA553087510

Gene: DMP1

Linked Data

• dbSNP Id: rs1374072029
• gnomAD v2: 4-88583063-T-C
• gnomAD v3: 4-87661911-T-C
• gnomAD v4: 4-87661911-T-C
• MyVariant Identifiers: chr4:g.88583063T>C (hg19) ; chr4:g.87661911T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87661911T>C , CM000666.2:g.87661911T>C	GRCh38
NC_000004.11:g.88583063T>C , CM000666.1:g.88583063T>C	GRCh37
NC_000004.10:g.88802087T>C	NCBI36
NG_008988.1:g.16610T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000282479.8:c.136-51T>C	ENSP00000282479.6:n.136-51T>C
ENST00000682752.1:c.*95-51T>C	ENSP00000507436.1:n.*95-51T>C
ENST00000682781.1:n.261-51T>C
ENST00000683764.1:n.456-51T>C
ENST00000684240.1:n.347-51T>C
ENST00000684389.1:n.308-51T>C
ENST00000339673.11:c.184-51T>C MANE Select	ENSP00000340935.6:n.184-51T>C
ENST00000282479.7:c.136-51T>C	ENSP00000282479.6:n.136-51T>C
ENST00000339673.10:c.184-51T>C	ENSP00000340935.6:n.184-51T>C
NM_001079911.2:c.136-51T>C	NP_001073380.1:n.136-51T>C
NM_004407.3:c.184-51T>C	NP_004398.1:n.184-51T>C
XM_011531705.1:c.271-51T>C	XP_011530007.1:n.271-51T>C
XM_011531706.1:c.223-51T>C	XP_011530008.1:n.223-51T>C
XR_938960.1:n.115-4502A>G
XM_011531705.2:c.271-51T>C	XP_011530007.1:n.271-51T>C
XM_011531706.2:c.223-51T>C	XP_011530008.1:n.223-51T>C
XR_938960.2:n.115-4502A>G
NM_001079911.3:c.136-51T>C	NP_001073380.1:n.136-51T>C
NM_004407.4:c.184-51T>C MANE Select	NP_004398.1:n.184-51T>C