Canonical Allele Identifier: CA357702716

Gene: DMP1

Linked Data

• MyVariant Identifiers: chr4:g.88584423A>C (hg19) ; chr4:g.87663271A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87663271A>C , CM000666.2:g.87663271A>C	GRCh38
NC_000004.11:g.88584423A>C , CM000666.1:g.88584423A>C	GRCh37
NC_000004.10:g.88803447A>C	NCBI36
NG_008988.1:g.17970A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282479.8:c.1445A>C	ENSP00000282479.6:p.Asn482Thr
ENST00000682752.1:c.*1404A>C	ENSP00000507436.1:n.*1404A>C
ENST00000682781.1:n.1570A>C
ENST00000683764.1:n.1765A>C
ENST00000684240.1:n.1656A>C
ENST00000684389.1:n.1617A>C
ENST00000339673.11:c.1493A>C MANE Select	ENSP00000340935.6:p.Asn498Thr
ENST00000282479.7:c.1445A>C	ENSP00000282479.6:p.Asn482Thr
ENST00000339673.10:c.1493A>C	ENSP00000340935.6:p.Asn498Thr
NM_001079911.2:c.1445A>C	NP_001073380.1:p.Asn482Thr
NM_004407.3:c.1493A>C	NP_004398.1:p.Asn498Thr
XM_011531705.1:c.1580A>C	XP_011530007.1:p.Asn527Thr
XM_011531706.1:c.1532A>C	XP_011530008.1:p.Asn511Thr
XR_938960.1:n.115-5862T>G
XM_011531705.2:c.1580A>C	XP_011530007.1:p.Asn527Thr
XM_011531706.2:c.1532A>C	XP_011530008.1:p.Asn511Thr
XR_938960.2:n.115-5862T>G
NM_001079911.3:c.1445A>C	NP_001073380.1:p.Asn482Thr
NM_004407.4:c.1493A>C MANE Select	NP_004398.1:p.Asn498Thr