Canonical Allele Identifier: CA357702870

Gene: DMP1

Linked Data

• MyVariant Identifiers: chr4:g.88584461G>T (hg19) ; chr4:g.87663309G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87663309G>T , CM000666.2:g.87663309G>T	GRCh38
NC_000004.11:g.88584461G>T , CM000666.1:g.88584461G>T	GRCh37
NC_000004.10:g.88803485G>T	NCBI36
NG_008988.1:g.18008G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282479.8:c.1483G>T	ENSP00000282479.6:p.Asp495Tyr
ENST00000682752.1:c.*1442G>T	ENSP00000507436.1:n.*1442G>T
ENST00000682781.1:n.1608G>T
ENST00000683764.1:n.1803G>T
ENST00000684240.1:n.1694G>T
ENST00000684389.1:n.1655G>T
ENST00000339673.11:c.1531G>T MANE Select	ENSP00000340935.6:p.Asp511Tyr
ENST00000282479.7:c.1483G>T	ENSP00000282479.6:p.Asp495Tyr
ENST00000339673.10:c.1531G>T	ENSP00000340935.6:p.Asp511Tyr
NM_001079911.2:c.1483G>T	NP_001073380.1:p.Asp495Tyr
NM_004407.3:c.1531G>T	NP_004398.1:p.Asp511Tyr
XM_011531705.1:c.1618G>T	XP_011530007.1:p.Asp540Tyr
XM_011531706.1:c.1570G>T	XP_011530008.1:p.Asp524Tyr
XR_938960.1:n.115-5900C>A
XM_011531705.2:c.1618G>T	XP_011530007.1:p.Asp540Tyr
XM_011531706.2:c.1570G>T	XP_011530008.1:p.Asp524Tyr
XR_938960.2:n.115-5900C>A
NM_001079911.3:c.1483G>T	NP_001073380.1:p.Asp495Tyr
NM_004407.4:c.1531G>T MANE Select	NP_004398.1:p.Asp511Tyr