Canonical Allele Identifier: CA101381905

Gene: DMP1

Linked Data

• dbSNP Id: rs986468886
• gnomAD v2: 4-88584486-A-T
• gnomAD v3: 4-87663334-A-T
• gnomAD v4: 4-87663334-A-T
• MyVariant Identifiers: chr4:g.88584486A>T (hg19) ; chr4:g.87663334A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87663334A>T , CM000666.2:g.87663334A>T	GRCh38
NC_000004.11:g.88584486A>T , CM000666.1:g.88584486A>T	GRCh37
NC_000004.10:g.88803510A>T	NCBI36
NG_008988.1:g.18033A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282479.8:c.*14A>T	ENSP00000282479.6:n.*14A>T
ENST00000682752.1:c.*1467A>T	ENSP00000507436.1:n.*1467A>T
ENST00000682781.1:n.1633A>T
ENST00000683764.1:n.1828A>T
ENST00000684240.1:n.1719A>T
ENST00000684389.1:n.1680A>T
ENST00000339673.11:c.*14A>T MANE Select	ENSP00000340935.6:n.*14A>T
ENST00000282479.7:c.*14A>T	ENSP00000282479.6:n.*14A>T
ENST00000339673.10:c.*14A>T	ENSP00000340935.6:n.*14A>T
NM_001079911.2:c.*14A>T	NP_001073380.1:n.*14A>T
NM_004407.3:c.*14A>T	NP_004398.1:n.*14A>T
XM_011531705.1:c.*14A>T	XP_011530007.1:n.*14A>T
XM_011531706.1:c.*14A>T	XP_011530008.1:n.*14A>T
XR_938960.1:n.115-5925T>A
XM_011531705.2:c.*14A>T	XP_011530007.1:n.*14A>T
XM_011531706.2:c.*14A>T	XP_011530008.1:n.*14A>T
XR_938960.2:n.115-5925T>A
NM_001079911.3:c.*14A>T	NP_001073380.1:n.*14A>T
NM_004407.4:c.*14A>T MANE Select	NP_004398.1:n.*14A>T