Canonical Allele Identifier: CA357702746

Gene: DMP1

Linked Data

• MyVariant Identifiers: chr4:g.88584432T>A (hg19) ; chr4:g.87663280T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87663280T>A , CM000666.2:g.87663280T>A	GRCh38
NC_000004.11:g.88584432T>A , CM000666.1:g.88584432T>A	GRCh37
NC_000004.10:g.88803456T>A	NCBI36
NG_008988.1:g.17979T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282479.8:c.1454T>A	ENSP00000282479.6:p.Ile485Asn
ENST00000682752.1:c.*1413T>A	ENSP00000507436.1:n.*1413T>A
ENST00000682781.1:n.1579T>A
ENST00000683764.1:n.1774T>A
ENST00000684240.1:n.1665T>A
ENST00000684389.1:n.1626T>A
ENST00000339673.11:c.1502T>A MANE Select	ENSP00000340935.6:p.Ile501Asn
ENST00000282479.7:c.1454T>A	ENSP00000282479.6:p.Ile485Asn
ENST00000339673.10:c.1502T>A	ENSP00000340935.6:p.Ile501Asn
NM_001079911.2:c.1454T>A	NP_001073380.1:p.Ile485Asn
NM_004407.3:c.1502T>A	NP_004398.1:p.Ile501Asn
XM_011531705.1:c.1589T>A	XP_011530007.1:p.Ile530Asn
XM_011531706.1:c.1541T>A	XP_011530008.1:p.Ile514Asn
XR_938960.1:n.115-5871A>T
XM_011531705.2:c.1589T>A	XP_011530007.1:p.Ile530Asn
XM_011531706.2:c.1541T>A	XP_011530008.1:p.Ile514Asn
XR_938960.2:n.115-5871A>T
NM_001079911.3:c.1454T>A	NP_001073380.1:p.Ile485Asn
NM_004407.4:c.1502T>A MANE Select	NP_004398.1:p.Ile501Asn