Canonical Allele Identifier: CA101381907

Gene: DMP1

Linked Data

• dbSNP Id: rs536209200
• gnomAD v4: 4-87663351-T-C
• MyVariant Identifiers: chr4:g.88584503T>C (hg19) ; chr4:g.87663351T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87663351T>C , CM000666.2:g.87663351T>C	GRCh38
NC_000004.11:g.88584503T>C , CM000666.1:g.88584503T>C	GRCh37
NC_000004.10:g.88803527T>C	NCBI36
NG_008988.1:g.18050T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282479.8:c.*31T>C	ENSP00000282479.6:n.*31T>C
ENST00000682752.1:c.*1484T>C	ENSP00000507436.1:n.*1484T>C
ENST00000682781.1:n.1650T>C
ENST00000683764.1:n.1845T>C
ENST00000684240.1:n.1736T>C
ENST00000684389.1:n.1697T>C
ENST00000339673.11:c.*31T>C MANE Select	ENSP00000340935.6:n.*31T>C
ENST00000282479.7:c.*31T>C	ENSP00000282479.6:n.*31T>C
ENST00000339673.10:c.*31T>C	ENSP00000340935.6:n.*31T>C
NM_001079911.2:c.*31T>C	NP_001073380.1:n.*31T>C
NM_004407.3:c.*31T>C	NP_004398.1:n.*31T>C
XM_011531705.1:c.*31T>C	XP_011530007.1:n.*31T>C
XM_011531706.1:c.*31T>C	XP_011530008.1:n.*31T>C
XR_938960.1:n.115-5942A>G
XM_011531705.2:c.*31T>C	XP_011530007.1:n.*31T>C
XM_011531706.2:c.*31T>C	XP_011530008.1:n.*31T>C
XR_938960.2:n.115-5942A>G
NM_001079911.3:c.*31T>C	NP_001073380.1:n.*31T>C
NM_004407.4:c.*31T>C MANE Select	NP_004398.1:n.*31T>C