Canonical Allele Identifier: CA2332763122

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33521772A= , CM000681.2:g.33521772A=	GRCh38
NC_000019.9:g.34012678A= , CM000681.1:g.34012678A=	GRCh37
NC_000019.8:g.38704518A=	NCBI36
NG_013358.1:g.5122T=
NG_013358.2:g.5122T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.-12T=	ENSP00000468516.4:n.-12T=
ENST00000651901.2:c.-12T=	ENSP00000498922.2:n.-12T=
ENST00000698359.1:c.-12T=	ENSP00000513682.1:n.-12T=
ENST00000698360.1:c.-12T=	ENSP00000513683.1:n.-12T=
ENST00000698361.1:c.-12T=	ENSP00000513684.1:n.-12T=
ENST00000698362.1:c.-12T=	ENSP00000513685.1:n.-12T=
ENST00000698363.1:n.52T=
ENST00000698364.1:n.52T=
ENST00000698365.1:n.52T=
ENST00000698426.1:c.-527T=	ENSP00000513713.1:n.-527T=
ENST00000698427.1:c.-77T=	ENSP00000513714.1:n.-77T=
ENST00000698428.1:c.-405T=	ENSP00000513715.1:n.-405T=
ENST00000698435.1:c.-12T=	ENSP00000513719.1:n.-12T=
ENST00000698436.1:c.-12T=	ENSP00000513720.1:n.-12T=
ENST00000244137.12:c.-12T= MANE Select	ENSP00000244137.5:n.-12T=
ENST00000244137.11:c.-12T=	ENSP00000244137.5:n.-12T=
ENST00000397032.8:c.-12T=	ENSP00000380226.3:n.-12T=
ENST00000436370.7:c.-12T=	ENSP00000391890.2:n.-12T=
NM_000285.3:c.-12T=	NP_000276.2:n.-12T=
NM_001166056.1:c.-12T=	NP_001159528.1:n.-12T=
NM_001166057.1:c.-12T=	NP_001159529.1:n.-12T=
NM_000285.4:c.-12T= MANE Select	NP_000276.2:n.-12T=
NM_001166056.2:c.-12T=	NP_001159528.1:n.-12T=
NM_001166057.2:c.-12T=	NP_001159529.1:n.-12T=