Canonical Allele Identifier: CA2332763158

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33521796T= , CM000681.2:g.33521796T=	GRCh38
NC_000019.9:g.34012702T= , CM000681.1:g.34012702T=	GRCh37
NC_000019.8:g.38704542T=	NCBI36
NG_013358.1:g.5098A=
NG_013358.2:g.5098A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698360.1:c.-36A=	ENSP00000513683.1:n.-36A=
ENST00000698361.1:c.-36A=	ENSP00000513684.1:n.-36A=
ENST00000698362.1:c.-36A=	ENSP00000513685.1:n.-36A=
ENST00000698363.1:n.28A=
ENST00000698364.1:n.28A=
ENST00000698365.1:n.28A=
ENST00000698436.1:c.-36A=	ENSP00000513720.1:n.-36A=
NM_000285.3:c.-36A=	NP_000276.2:n.-36A=
NM_001166056.1:c.-36A=	NP_001159528.1:n.-36A=
NM_001166057.1:c.-36A=	NP_001159529.1:n.-36A=