Canonical Allele Identifier: CA381436974

Gene: DPP3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66487343G>A , CM000673.2:g.66487343G>A	GRCh38
NC_000011.9:g.66254814G>A , CM000673.1:g.66254814G>A	GRCh37
NC_000011.8:g.66011390G>A	NCBI36
NG_032068.1:g.11935G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531863.6:c.573+1G>A MANE Select	ENSP00000432782.2:n.573+1G>A
ENST00000526515.5:c.483+1G>A	ENSP00000431606.1:n.483+1G>A
ENST00000530165.5:c.483+1G>A	ENSP00000436941.1:n.483+1G>A
ENST00000531354.2:c.573+1G>A	ENSP00000432618.2:n.573+1G>A
ENST00000531863.5:c.633+1G>A	ENSP00000432782.1:n.633+1G>A
ENST00000532019.5:c.267+1G>A	ENSP00000437101.1:n.267+1G>A
ENST00000532677.5:c.630+1G>A	ENSP00000435284.1:n.630+1G>A
ENST00000533725.5:c.267+1G>A	ENSP00000434518.1:n.267+1G>A
ENST00000541961.5:c.573+1G>A	ENSP00000440502.1:n.573+1G>A
NM_001256670.1:c.483+1G>A	NP_001243599.1:n.483+1G>A
NM_005700.4:c.573+1G>A	NP_005691.2:n.573+1G>A
NM_130443.3:c.573+1G>A	NP_569710.2:n.573+1G>A
NM_001256670.2:c.483+1G>A	NP_001243599.1:n.483+1G>A
NM_005700.5:c.573+1G>A	NP_005691.2:n.573+1G>A
NM_130443.4:c.573+1G>A MANE Select	NP_569710.2:n.573+1G>A