Canonical Allele Identifier: CA357697462

Gene: DMP1

Linked Data

• MyVariant Identifiers: chr4:g.88577652T>A (hg19) ; chr4:g.87656500T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87656500T>A , CM000666.2:g.87656500T>A	GRCh38
NC_000004.11:g.88577652T>A , CM000666.1:g.88577652T>A	GRCh37
NC_000004.10:g.88796676T>A	NCBI36
NG_008988.1:g.11199T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000282479.8:c.8T>A	ENSP00000282479.6:p.Ile3Asn
ENST00000682752.1:c.8T>A	ENSP00000507436.1:p.Ile3Asn
ENST00000682781.1:n.133T>A
ENST00000683764.1:n.171T>A
ENST00000684240.1:n.171T>A
ENST00000684389.1:n.132T>A
ENST00000339673.11:c.8T>A MANE Select	ENSP00000340935.6:p.Ile3Asn
ENST00000282479.7:c.8T>A	ENSP00000282479.6:p.Ile3Asn
ENST00000339673.10:c.8T>A	ENSP00000340935.6:p.Ile3Asn
NM_001079911.2:c.8T>A	NP_001073380.1:p.Ile3Asn
NM_004407.3:c.8T>A	NP_004398.1:p.Ile3Asn
XM_011531705.1:c.95T>A	XP_011530007.1:p.Ile32Asn
XM_011531706.1:c.95T>A	XP_011530008.1:p.Ile32Asn
XM_011531705.2:c.95T>A	XP_011530007.1:p.Ile32Asn
XM_011531706.2:c.95T>A	XP_011530008.1:p.Ile32Asn
NM_001079911.3:c.8T>A	NP_001073380.1:p.Ile3Asn
NM_004407.4:c.8T>A MANE Select	NP_004398.1:p.Ile3Asn