Canonical Allele Identifier: CA2814189177

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33521787A>G , CM000681.2:g.33521787A>G	GRCh38
NC_000019.9:g.34012693A>G , CM000681.1:g.34012693A>G	GRCh37
NC_000019.8:g.38704533A>G	NCBI36
NG_013358.1:g.5107T>C
NG_013358.2:g.5107T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.-27T>C	ENSP00000468516.4:n.-27T>C
ENST00000651901.2:c.-27T>C	ENSP00000498922.2:n.-27T>C
ENST00000698359.1:c.-27T>C	ENSP00000513682.1:n.-27T>C
ENST00000698360.1:c.-27T>C	ENSP00000513683.1:n.-27T>C
ENST00000698361.1:c.-27T>C	ENSP00000513684.1:n.-27T>C
ENST00000698362.1:c.-27T>C	ENSP00000513685.1:n.-27T>C
ENST00000698363.1:n.37T>C
ENST00000698364.1:n.37T>C
ENST00000698365.1:n.37T>C
ENST00000698428.1:c.-420T>C	ENSP00000513715.1:n.-420T>C
ENST00000698435.1:c.-27T>C	ENSP00000513719.1:n.-27T>C
ENST00000698436.1:c.-27T>C	ENSP00000513720.1:n.-27T>C
ENST00000244137.12:c.-27T>C MANE Select	ENSP00000244137.5:n.-27T>C
ENST00000244137.11:c.-27T>C	ENSP00000244137.5:n.-27T>C
ENST00000397032.8:c.-27T>C	ENSP00000380226.3:n.-27T>C
ENST00000436370.7:c.-27T>C	ENSP00000391890.2:n.-27T>C
NM_000285.3:c.-27T>C	NP_000276.2:n.-27T>C
NM_001166056.1:c.-27T>C	NP_001159528.1:n.-27T>C
NM_001166057.1:c.-27T>C	NP_001159529.1:n.-27T>C
NM_000285.4:c.-27T>C MANE Select	NP_000276.2:n.-27T>C
NM_001166056.2:c.-27T>C	NP_001159528.1:n.-27T>C
NM_001166057.2:c.-27T>C	NP_001159529.1:n.-27T>C