Canonical Allele Identifier: CA101381482
Community Standard Title: NM_004407.4(DMP1):c.103-318A>G
Gene: DMP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87658902A>G , CM000666.2:g.87658902A>G GRCh38
NC_000004.11:g.88580054A>G , CM000666.1:g.88580054A>G GRCh37
NC_000004.10:g.88799078A>G NCBI36
NG_008988.1:g.13601A>G

Transcript Alleles

HGVS Amino-acid Change
NM_004407.4:c.103-318A>G MANE Select NP_004398.1:n.103-318A>G
ENST00000339673.11:c.103-318A>G MANE Select ENSP00000340935.6:n.103-318A>G
NM_001079911.2:c.103-318A>G NP_001073380.1:n.103-318A>G
NM_001079911.3:c.103-318A>G NP_001073380.1:n.103-318A>G
NM_004407.3:c.103-318A>G NP_004398.1:n.103-318A>G
ENST00000282479.7:c.103-318A>G ENSP00000282479.6:n.103-318A>G
ENST00000282479.8:c.103-318A>G ENSP00000282479.6:n.103-318A>G
ENST00000339673.10:c.103-318A>G ENSP00000340935.6:n.103-318A>G
ENST00000682752.1:c.103-318A>G ENSP00000507436.1:n.103-318A>G
ENST00000682781.1:n.228-318A>G
ENST00000683764.1:n.266-318A>G
ENST00000684240.1:n.266-318A>G
ENST00000684389.1:n.227-318A>G
XM_011531705.1:c.190-318A>G XP_011530007.1:n.190-318A>G
XM_011531705.2:c.190-318A>G XP_011530007.1:n.190-318A>G
XM_011531706.1:c.190-318A>G XP_011530008.1:n.190-318A>G
XM_011531706.2:c.190-318A>G XP_011530008.1:n.190-318A>G
XR_938960.1:n.115-1493T>C
XR_938960.2:n.115-1493T>C