Canonical Allele Identifier: CA357702826

Gene: DMP1

Linked Data

• MyVariant Identifiers: chr4:g.88584451T>G (hg19) ; chr4:g.87663299T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87663299T>G , CM000666.2:g.87663299T>G	GRCh38
NC_000004.11:g.88584451T>G , CM000666.1:g.88584451T>G	GRCh37
NC_000004.10:g.88803475T>G	NCBI36
NG_008988.1:g.17998T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282479.8:c.1473T>G	ENSP00000282479.6:p.Asn491Lys
ENST00000682752.1:c.*1432T>G	ENSP00000507436.1:n.*1432T>G
ENST00000682781.1:n.1598T>G
ENST00000683764.1:n.1793T>G
ENST00000684240.1:n.1684T>G
ENST00000684389.1:n.1645T>G
ENST00000339673.11:c.1521T>G MANE Select	ENSP00000340935.6:p.Asn507Lys
ENST00000282479.7:c.1473T>G	ENSP00000282479.6:p.Asn491Lys
ENST00000339673.10:c.1521T>G	ENSP00000340935.6:p.Asn507Lys
NM_001079911.2:c.1473T>G	NP_001073380.1:p.Asn491Lys
NM_004407.3:c.1521T>G	NP_004398.1:p.Asn507Lys
XM_011531705.1:c.1608T>G	XP_011530007.1:p.Asn536Lys
XM_011531706.1:c.1560T>G	XP_011530008.1:p.Asn520Lys
XR_938960.1:n.115-5890A>C
XM_011531705.2:c.1608T>G	XP_011530007.1:p.Asn536Lys
XM_011531706.2:c.1560T>G	XP_011530008.1:p.Asn520Lys
XR_938960.2:n.115-5890A>C
NM_001079911.3:c.1473T>G	NP_001073380.1:p.Asn491Lys
NM_004407.4:c.1521T>G MANE Select	NP_004398.1:p.Asn507Lys