Canonical Allele Identifier: CA357702711

Gene: DMP1

Linked Data

• MyVariant Identifiers: chr4:g.88584421C>G (hg19) ; chr4:g.87663269C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87663269C>G , CM000666.2:g.87663269C>G	GRCh38
NC_000004.11:g.88584421C>G , CM000666.1:g.88584421C>G	GRCh37
NC_000004.10:g.88803445C>G	NCBI36
NG_008988.1:g.17968C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282479.8:c.1443C>G	ENSP00000282479.6:p.His481Gln
ENST00000682752.1:c.*1402C>G	ENSP00000507436.1:n.*1402C>G
ENST00000682781.1:n.1568C>G
ENST00000683764.1:n.1763C>G
ENST00000684240.1:n.1654C>G
ENST00000684389.1:n.1615C>G
ENST00000339673.11:c.1491C>G MANE Select	ENSP00000340935.6:p.His497Gln
ENST00000282479.7:c.1443C>G	ENSP00000282479.6:p.His481Gln
ENST00000339673.10:c.1491C>G	ENSP00000340935.6:p.His497Gln
NM_001079911.2:c.1443C>G	NP_001073380.1:p.His481Gln
NM_004407.3:c.1491C>G	NP_004398.1:p.His497Gln
XM_011531705.1:c.1578C>G	XP_011530007.1:p.His526Gln
XM_011531706.1:c.1530C>G	XP_011530008.1:p.His510Gln
XR_938960.1:n.115-5860G>C
XM_011531705.2:c.1578C>G	XP_011530007.1:p.His526Gln
XM_011531706.2:c.1530C>G	XP_011530008.1:p.His510Gln
XR_938960.2:n.115-5860G>C
NM_001079911.3:c.1443C>G	NP_001073380.1:p.His481Gln
NM_004407.4:c.1491C>G MANE Select	NP_004398.1:p.His497Gln