Canonical Allele Identifier: CA101381851
Gene: DMP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87662587A>C , CM000666.2:g.87662587A>C GRCh38
NC_000004.11:g.88583739A>C , CM000666.1:g.88583739A>C GRCh37
NC_000004.10:g.88802763A>C NCBI36
NG_008988.1:g.17286A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282479.8:c.761A>C ENSP00000282479.6:p.Lys254Thr
ENST00000682752.1:c.*720A>C ENSP00000507436.1:n.*720A>C
ENST00000682781.1:n.886A>C
ENST00000683764.1:n.1081A>C
ENST00000684240.1:n.972A>C
ENST00000684389.1:n.933A>C
ENST00000339673.11:c.809A>C MANE Select ENSP00000340935.6:p.Lys270Thr
ENST00000282479.7:c.761A>C ENSP00000282479.6:p.Lys254Thr
ENST00000339673.10:c.809A>C ENSP00000340935.6:p.Lys270Thr
NM_001079911.2:c.761A>C NP_001073380.1:p.Lys254Thr
NM_004407.3:c.809A>C NP_004398.1:p.Lys270Thr
XM_011531705.1:c.896A>C XP_011530007.1:p.Lys299Thr
XM_011531706.1:c.848A>C XP_011530008.1:p.Lys283Thr
XR_938960.1:n.115-5178T>G
XM_011531705.2:c.896A>C XP_011530007.1:p.Lys299Thr
XM_011531706.2:c.848A>C XP_011530008.1:p.Lys283Thr
XR_938960.2:n.115-5178T>G
NM_001079911.3:c.761A>C NP_001073380.1:p.Lys254Thr
NM_004407.4:c.809A>C MANE Select NP_004398.1:p.Lys270Thr