Canonical Allele Identifier: CA101381863

Gene: DMP1

Linked Data

• ClinVar Variation Id: 505906
• ClinVar RCV Id: RCV000609230
• dbSNP Id: rs899142959
• MyVariant Identifiers: chr4:g.88583909C>T (hg19) ; chr4:g.87662757C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87662757C>T , CM000666.2:g.87662757C>T	GRCh38
NC_000004.11:g.88583909C>T , CM000666.1:g.88583909C>T	GRCh37
NC_000004.10:g.88802933C>T	NCBI36
NG_008988.1:g.17456C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282479.8:c.931C>T	ENSP00000282479.6:p.Gln311Ter
ENST00000682752.1:c.*890C>T	ENSP00000507436.1:n.*890C>T
ENST00000682781.1:n.1056C>T
ENST00000683764.1:n.1251C>T
ENST00000684240.1:n.1142C>T
ENST00000684389.1:n.1103C>T
ENST00000339673.11:c.979C>T MANE Select	ENSP00000340935.6:p.Gln327Ter
ENST00000282479.7:c.931C>T	ENSP00000282479.6:p.Gln311Ter
ENST00000339673.10:c.979C>T	ENSP00000340935.6:p.Gln327Ter
NM_001079911.2:c.931C>T	NP_001073380.1:p.Gln311Ter
NM_004407.3:c.979C>T	NP_004398.1:p.Gln327Ter
XM_011531705.1:c.1066C>T	XP_011530007.1:p.Gln356Ter
XM_011531706.1:c.1018C>T	XP_011530008.1:p.Gln340Ter
XR_938960.1:n.115-5348G>A
XM_011531705.2:c.1066C>T	XP_011530007.1:p.Gln356Ter
XM_011531706.2:c.1018C>T	XP_011530008.1:p.Gln340Ter
XR_938960.2:n.115-5348G>A
NM_001079911.3:c.931C>T	NP_001073380.1:p.Gln311Ter
NM_004407.4:c.979C>T MANE Select	NP_004398.1:p.Gln327Ter