Canonical Allele Identifier: CA440287952

Gene: DMP1

Linked Data

• gnomAD v4: 4-87663278-C-A
• MyVariant Identifiers: chr4:g.88584430C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87663278C>A , CM000666.2:g.87663278C>A	GRCh38
NC_000004.11:g.88584430C>A , CM000666.1:g.88584430C>A	GRCh37
NC_000004.10:g.88803454C>A	NCBI36
NG_008988.1:g.17977C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282479.8:c.1452C>A	ENSP00000282479.6:p.Pro484=
ENST00000682752.1:c.*1411C>A	ENSP00000507436.1:n.*1411C>A
ENST00000682781.1:n.1577C>A
ENST00000683764.1:n.1772C>A
ENST00000684240.1:n.1663C>A
ENST00000684389.1:n.1624C>A
ENST00000339673.11:c.1500C>A MANE Select	ENSP00000340935.6:p.Pro500=
ENST00000282479.7:c.1452C>A	ENSP00000282479.6:p.Pro484=
ENST00000339673.10:c.1500C>A	ENSP00000340935.6:p.Pro500=
NM_001079911.2:c.1452C>A	NP_001073380.1:p.Pro484=
NM_004407.3:c.1500C>A	NP_004398.1:p.Pro500=
XM_011531705.1:c.1587C>A	XP_011530007.1:p.Pro529=
XM_011531706.1:c.1539C>A	XP_011530008.1:p.Pro513=
XR_938960.1:n.115-5869G>T
XM_011531705.2:c.1587C>A	XP_011530007.1:p.Pro529=
XM_011531706.2:c.1539C>A	XP_011530008.1:p.Pro513=
XR_938960.2:n.115-5869G>T
NM_001079911.3:c.1452C>A	NP_001073380.1:p.Pro484=
NM_004407.4:c.1500C>A MANE Select	NP_004398.1:p.Pro500=