Canonical Allele Identifier: CA357697474

Gene: DMP1

Linked Data

• MyVariant Identifiers: chr4:g.88577657A>G (hg19) ; chr4:g.87656505A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87656505A>G , CM000666.2:g.87656505A>G	GRCh38
NC_000004.11:g.88577657A>G , CM000666.1:g.88577657A>G	GRCh37
NC_000004.10:g.88796681A>G	NCBI36
NG_008988.1:g.11204A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000282479.8:c.13A>G	ENSP00000282479.6:p.Ile5Val
ENST00000682752.1:c.13A>G	ENSP00000507436.1:p.Ile5Val
ENST00000682781.1:n.138A>G
ENST00000683764.1:n.176A>G
ENST00000684240.1:n.176A>G
ENST00000684389.1:n.137A>G
ENST00000339673.11:c.13A>G MANE Select	ENSP00000340935.6:p.Ile5Val
ENST00000282479.7:c.13A>G	ENSP00000282479.6:p.Ile5Val
ENST00000339673.10:c.13A>G	ENSP00000340935.6:p.Ile5Val
NM_001079911.2:c.13A>G	NP_001073380.1:p.Ile5Val
NM_004407.3:c.13A>G	NP_004398.1:p.Ile5Val
XM_011531705.1:c.100A>G	XP_011530007.1:p.Ile34Val
XM_011531706.1:c.100A>G	XP_011530008.1:p.Ile34Val
XM_011531705.2:c.100A>G	XP_011530007.1:p.Ile34Val
XM_011531706.2:c.100A>G	XP_011530008.1:p.Ile34Val
NM_001079911.3:c.13A>G	NP_001073380.1:p.Ile5Val
NM_004407.4:c.13A>G MANE Select	NP_004398.1:p.Ile5Val