Canonical Allele Identifier: CA9363913

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387877C>T , CM000681.2:g.33387877C>T	GRCh38
NC_000019.9:g.33878783C>T , CM000681.1:g.33878783C>T	GRCh37
NC_000019.8:g.38570623C>T	NCBI36
NG_013358.1:g.139017G>A
NG_013358.2:g.139017G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000285.4:c.1344+13G>A MANE Select	NP_000276.2:n.1344+13G>A
ENST00000244137.12:c.1344+13G>A MANE Select	ENSP00000244137.5:n.1344+13G>A
NM_000285.3:c.1344+13G>A	NP_000276.2:n.1344+13G>A
NM_001166056.1:c.1221+13G>A	NP_001159528.1:n.1221+13G>A
NM_001166056.2:c.1221+13G>A	NP_001159528.1:n.1221+13G>A
NM_001166057.1:c.1152+13G>A	NP_001159529.1:n.1152+13G>A
NM_001166057.2:c.1152+13G>A	NP_001159529.1:n.1152+13G>A
ENST00000244137.11:c.1344+13G>A	ENSP00000244137.5:n.1344+13G>A
ENST00000397032.8:c.1221+13G>A	ENSP00000380226.3:n.1221+13G>A
ENST00000436370.7:c.1152+13G>A	ENSP00000391890.2:n.1152+13G>A
ENST00000588328.6:c.1399+13G>A
ENST00000588328.7:c.1410+13G>A	ENSP00000468516.4:n.1410+13G>A
ENST00000591968.1:n.416+13G>A
ENST00000593085.1:n.1231+13G>A
ENST00000651901.1:c.1340+13G>A
ENST00000651901.2:c.1344+13G>A	ENSP00000498922.2:n.1344+13G>A
ENST00000698359.1:c.1299+13G>A	ENSP00000513682.1:n.1299+13G>A
ENST00000698360.1:c.1395+13G>A	ENSP00000513683.1:n.1395+13G>A
ENST00000698361.1:c.1460+13G>A	ENSP00000513684.1:n.1460+13G>A
ENST00000698362.1:c.*86G>A	ENSP00000513685.1:n.*86G>A
ENST00000698426.1:c.1023+13G>A	ENSP00000513713.1:n.1023+13G>A
ENST00000698427.1:c.1386+13G>A	ENSP00000513714.1:n.1386+13G>A
ENST00000698428.1:c.1023+13G>A	ENSP00000513715.1:n.1023+13G>A
ENST00000698429.1:n.1227+13G>A
ENST00000698430.1:c.1594+13G>A
ENST00000698431.1:c.1081+13G>A	ENSP00000513717.1:n.1081+13G>A
ENST00000698432.1:c.1153+13G>A
ENST00000698433.1:n.806+13G>A