Canonical Allele Identifier: CA357697455

Gene: DMP1

Linked Data

• MyVariant Identifiers: chr4:g.88577649A>G (hg19) ; chr4:g.87656497A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87656497A>G , CM000666.2:g.87656497A>G	GRCh38
NC_000004.11:g.88577649A>G , CM000666.1:g.88577649A>G	GRCh37
NC_000004.10:g.88796673A>G	NCBI36
NG_008988.1:g.11196A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000282479.8:c.5A>G	ENSP00000282479.6:p.Lys2Arg
ENST00000682752.1:c.5A>G	ENSP00000507436.1:p.Lys2Arg
ENST00000682781.1:n.130A>G
ENST00000683764.1:n.168A>G
ENST00000684240.1:n.168A>G
ENST00000684389.1:n.129A>G
ENST00000339673.11:c.5A>G MANE Select	ENSP00000340935.6:p.Lys2Arg
ENST00000282479.7:c.5A>G	ENSP00000282479.6:p.Lys2Arg
ENST00000339673.10:c.5A>G	ENSP00000340935.6:p.Lys2Arg
NM_001079911.2:c.5A>G	NP_001073380.1:p.Lys2Arg
NM_004407.3:c.5A>G	NP_004398.1:p.Lys2Arg
XM_011531705.1:c.92A>G	XP_011530007.1:p.Lys31Arg
XM_011531706.1:c.92A>G	XP_011530008.1:p.Lys31Arg
XM_011531705.2:c.92A>G	XP_011530007.1:p.Lys31Arg
XM_011531706.2:c.92A>G	XP_011530008.1:p.Lys31Arg
NM_001079911.3:c.5A>G	NP_001073380.1:p.Lys2Arg
NM_004407.4:c.5A>G MANE Select	NP_004398.1:p.Lys2Arg