Canonical Allele Identifier: CA440285036

Gene: DMP1

Linked Data

• gnomAD v4: 4-87656501-C-A
• MyVariant Identifiers: chr4:g.88577653C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87656501C>A , CM000666.2:g.87656501C>A	GRCh38
NC_000004.11:g.88577653C>A , CM000666.1:g.88577653C>A	GRCh37
NC_000004.10:g.88796677C>A	NCBI36
NG_008988.1:g.11200C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000282479.8:c.9C>A	ENSP00000282479.6:p.Ile3=
ENST00000682752.1:c.9C>A	ENSP00000507436.1:p.Ile3=
ENST00000682781.1:n.134C>A
ENST00000683764.1:n.172C>A
ENST00000684240.1:n.172C>A
ENST00000684389.1:n.133C>A
ENST00000339673.11:c.9C>A MANE Select	ENSP00000340935.6:p.Ile3=
ENST00000282479.7:c.9C>A	ENSP00000282479.6:p.Ile3=
ENST00000339673.10:c.9C>A	ENSP00000340935.6:p.Ile3=
NM_001079911.2:c.9C>A	NP_001073380.1:p.Ile3=
NM_004407.3:c.9C>A	NP_004398.1:p.Ile3=
XM_011531705.1:c.96C>A	XP_011530007.1:p.Ile32=
XM_011531706.1:c.96C>A	XP_011530008.1:p.Ile32=
XM_011531705.2:c.96C>A	XP_011530007.1:p.Ile32=
XM_011531706.2:c.96C>A	XP_011530008.1:p.Ile32=
NM_001079911.3:c.9C>A	NP_001073380.1:p.Ile3=
NM_004407.4:c.9C>A MANE Select	NP_004398.1:p.Ile3=