Canonical Allele Identifier: CA1474407303

Gene: DMP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87663272C= , CM000666.2:g.87663272C=	GRCh38
NC_000004.11:g.88584424C= , CM000666.1:g.88584424C=	GRCh37
NC_000004.10:g.88803448C=	NCBI36
NG_008988.1:g.17971C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282479.8:c.1446C=	ENSP00000282479.6:p.Asn482=
ENST00000682752.1:c.*1405C=	ENSP00000507436.1:n.*1405C=
ENST00000682781.1:n.1571C=
ENST00000683764.1:n.1766C=
ENST00000684240.1:n.1657C=
ENST00000684389.1:n.1618C=
ENST00000339673.11:c.1494C= MANE Select	ENSP00000340935.6:p.Asn498=
ENST00000282479.7:c.1446C=	ENSP00000282479.6:p.Asn482=
ENST00000339673.10:c.1494C=	ENSP00000340935.6:p.Asn498=
NM_001079911.2:c.1446C=	NP_001073380.1:p.Asn482=
NM_004407.3:c.1494C=	NP_004398.1:p.Asn498=
XM_011531705.1:c.1581C=	XP_011530007.1:p.Asn527=
XM_011531706.1:c.1533C=	XP_011530008.1:p.Asn511=
XR_938960.1:n.115-5863G=
XM_011531705.2:c.1581C=	XP_011530007.1:p.Asn527=
XM_011531706.2:c.1533C=	XP_011530008.1:p.Asn511=
XR_938960.2:n.115-5863G=
NM_001079911.3:c.1446C=	NP_001073380.1:p.Asn482=
NM_004407.4:c.1494C= MANE Select	NP_004398.1:p.Asn498=