Canonical Allele Identifier: CA725750403

Gene: DPEP1

Linked Data

• dbSNP Id: rs1356526750
• MyVariant Identifiers: chr16:g.89681147G>A (hg19) ; chr16:g.89614739G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89614739G>A , CM000678.2:g.89614739G>A	GRCh38
NC_000016.9:g.89681147G>A , CM000678.1:g.89681147G>A	GRCh37
NC_000016.8:g.88208648G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690203.1:c.-107+1020G>A MANE Select	ENSP00000508584.1:n.-107+1020G>A
ENST00000421184.5:c.-107+1335G>A	ENSP00000397313.1:n.-107+1335G>A
ENST00000564281.5:n.47+1020G>A
ENST00000565249.5:n.171+1020G>A
ENST00000570029.5:c.-107+1335G>A	ENSP00000455916.1:n.-107+1335G>A
NM_001128141.2:c.-107+1335G>A	NP_001121613.1:n.-107+1335G>A
XM_005256285.3:c.-107+1020G>A	XP_005256342.1:n.-107+1020G>A
XM_011522926.1:c.-107+1020G>A	XP_011521228.1:n.-107+1020G>A
XM_005256285.5:c.-107+1020G>A	XP_005256342.1:n.-107+1020G>A
NM_001128141.3:c.-107+1335G>A	NP_001121613.1:n.-107+1335G>A
NM_001389466.1:c.-107+1020G>A MANE Select	NP_001376395.1:n.-107+1020G>A
NM_001389470.1:c.-107+1020G>A	NP_001376399.1:n.-107+1020G>A