Canonical Allele Identifier: CA357702720

Gene: DMP1

Linked Data

• MyVariant Identifiers: chr4:g.88584424C>A (hg19) ; chr4:g.87663272C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87663272C>A , CM000666.2:g.87663272C>A	GRCh38
NC_000004.11:g.88584424C>A , CM000666.1:g.88584424C>A	GRCh37
NC_000004.10:g.88803448C>A	NCBI36
NG_008988.1:g.17971C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282479.8:c.1446C>A	ENSP00000282479.6:p.Asn482Lys
ENST00000682752.1:c.*1405C>A	ENSP00000507436.1:n.*1405C>A
ENST00000682781.1:n.1571C>A
ENST00000683764.1:n.1766C>A
ENST00000684240.1:n.1657C>A
ENST00000684389.1:n.1618C>A
ENST00000339673.11:c.1494C>A MANE Select	ENSP00000340935.6:p.Asn498Lys
ENST00000282479.7:c.1446C>A	ENSP00000282479.6:p.Asn482Lys
ENST00000339673.10:c.1494C>A	ENSP00000340935.6:p.Asn498Lys
NM_001079911.2:c.1446C>A	NP_001073380.1:p.Asn482Lys
NM_004407.3:c.1494C>A	NP_004398.1:p.Asn498Lys
XM_011531705.1:c.1581C>A	XP_011530007.1:p.Asn527Lys
XM_011531706.1:c.1533C>A	XP_011530008.1:p.Asn511Lys
XR_938960.1:n.115-5863G>T
XM_011531705.2:c.1581C>A	XP_011530007.1:p.Asn527Lys
XM_011531706.2:c.1533C>A	XP_011530008.1:p.Asn511Lys
XR_938960.2:n.115-5863G>T
NM_001079911.3:c.1446C>A	NP_001073380.1:p.Asn482Lys
NM_004407.4:c.1494C>A MANE Select	NP_004398.1:p.Asn498Lys