Canonical Allele Identifier: CA286586602

Gene: DPEP1

Linked Data

• dbSNP Id: rs1029945579
• gnomAD v2: 16-89680871-A-C
• gnomAD v3: 16-89614463-A-C
• gnomAD v4: 16-89614463-A-C
• MyVariant Identifiers: chr16:g.89680871A>C (hg19) ; chr16:g.89614463A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89614463A>C , CM000678.2:g.89614463A>C	GRCh38
NC_000016.9:g.89680871A>C , CM000678.1:g.89680871A>C	GRCh37
NC_000016.8:g.88208372A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000690203.1:c.-107+744A>C MANE Select	ENSP00000508584.1:n.-107+744A>C
ENST00000421184.5:c.-107+1059A>C	ENSP00000397313.1:n.-107+1059A>C
ENST00000564281.5:n.47+744A>C
ENST00000565249.5:n.171+744A>C
ENST00000570029.5:c.-107+1059A>C	ENSP00000455916.1:n.-107+1059A>C
NM_001128141.2:c.-107+1059A>C	NP_001121613.1:n.-107+1059A>C
XM_005256285.3:c.-107+744A>C	XP_005256342.1:n.-107+744A>C
XM_011522926.1:c.-107+744A>C	XP_011521228.1:n.-107+744A>C
XM_005256285.5:c.-107+744A>C	XP_005256342.1:n.-107+744A>C
NM_001128141.3:c.-107+1059A>C	NP_001121613.1:n.-107+1059A>C
NM_001389466.1:c.-107+744A>C MANE Select	NP_001376395.1:n.-107+744A>C
NM_001389470.1:c.-107+744A>C	NP_001376399.1:n.-107+744A>C