Canonical Allele Identifier: CA440287949

Gene: DMP1

Linked Data

• MyVariant Identifiers: chr4:g.88584421C>T (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000282479.8:c.1443C>T	ENSP00000282479.6:p.His481=
ENST00000682752.1:c.*1402C>T	ENSP00000507436.1:n.*1402C>T
ENST00000682781.1:n.1568C>T
ENST00000683764.1:n.1763C>T
ENST00000684240.1:n.1654C>T
ENST00000684389.1:n.1615C>T
ENST00000339673.11:c.1491C>T MANE Select	ENSP00000340935.6:p.His497=
ENST00000282479.7:c.1443C>T	ENSP00000282479.6:p.His481=
ENST00000339673.10:c.1491C>T	ENSP00000340935.6:p.His497=
NM_001079911.2:c.1443C>T	NP_001073380.1:p.His481=
NM_004407.3:c.1491C>T	NP_004398.1:p.His497=
XM_011531705.1:c.1578C>T	XP_011530007.1:p.His526=
XM_011531706.1:c.1530C>T	XP_011530008.1:p.His510=
XR_938960.1:n.115-5860G>A
XM_011531705.2:c.1578C>T	XP_011530007.1:p.His526=
XM_011531706.2:c.1530C>T	XP_011530008.1:p.His510=
XR_938960.2:n.115-5860G>A
NM_001079911.3:c.1443C>T	NP_001073380.1:p.His481=
NM_004407.4:c.1491C>T MANE Select	NP_004398.1:p.His497=