Canonical Allele Identifier: CA1065101216

Gene: DMP1

Linked Data

• dbSNP Id: rs1728690852
• gnomAD v3: 4-87656327-T-C
• gnomAD v4: 4-87656327-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87656327T>C , CM000666.2:g.87656327T>C	GRCh38
NC_000004.11:g.88577479T>C , CM000666.1:g.88577479T>C	GRCh37
NC_000004.10:g.88796503T>C	NCBI36
NG_008988.1:g.11026T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282479.8:c.-21-145T>C	ENSP00000282479.6:n.-21-145T>C
ENST00000682752.1:c.-21-145T>C	ENSP00000507436.1:n.-21-145T>C
ENST00000682781.1:n.105-145T>C
ENST00000683764.1:n.143-145T>C
ENST00000684240.1:n.143-145T>C
ENST00000684389.1:n.104-145T>C
ENST00000339673.11:c.-21-145T>C MANE Select	ENSP00000340935.6:n.-21-145T>C
ENST00000282479.7:c.-21-145T>C	ENSP00000282479.6:n.-21-145T>C
ENST00000339673.10:c.-21-145T>C	ENSP00000340935.6:n.-21-145T>C
NM_001079911.2:c.-21-145T>C	NP_001073380.1:n.-21-145T>C
NM_004407.3:c.-21-145T>C	NP_004398.1:n.-21-145T>C
XM_011531705.1:c.67-145T>C	XP_011530007.1:n.67-145T>C
XM_011531706.1:c.67-145T>C	XP_011530008.1:n.67-145T>C
XM_011531705.2:c.67-145T>C	XP_011530007.1:n.67-145T>C
XM_011531706.2:c.67-145T>C	XP_011530008.1:n.67-145T>C
NM_001079911.3:c.-21-145T>C	NP_001073380.1:n.-21-145T>C
NM_004407.4:c.-21-145T>C MANE Select	NP_004398.1:n.-21-145T>C