Canonical Allele Identifier: CA506687811

Gene: PEPD

Linked Data

• MyVariant Identifiers: chr19:g.33892658G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33401752G>A , CM000681.2:g.33401752G>A	GRCh38
NC_000019.9:g.33892658G>A , CM000681.1:g.33892658G>A	GRCh37
NC_000019.8:g.38584498G>A	NCBI36
NG_013358.1:g.125142C>T
NG_013358.2:g.125142C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.936C>T	ENSP00000468516.4:p.Ser312=
ENST00000651901.2:c.936C>T	ENSP00000498922.2:p.Ser312=
ENST00000698359.1:c.891C>T	ENSP00000513682.1:p.Ser297=
ENST00000698360.1:c.987C>T	ENSP00000513683.1:p.Ser329=
ENST00000698361.1:c.936C>T	ENSP00000513684.1:p.Ser312=
ENST00000698362.1:c.936C>T	ENSP00000513685.1:p.Ser312=
ENST00000698363.1:n.999C>T
ENST00000698364.1:n.999C>T
ENST00000698365.1:n.999C>T
ENST00000698426.1:c.615C>T	ENSP00000513713.1:p.Ser205=
ENST00000698427.1:c.978C>T	ENSP00000513714.1:p.Ser326=
ENST00000698428.1:c.615C>T	ENSP00000513715.1:p.Ser205=
ENST00000698429.1:n.819C>T
ENST00000698430.1:c.1186C>T
ENST00000698431.1:c.673C>T	ENSP00000513717.1:n.673C>T
ENST00000698432.1:c.745C>T
ENST00000698433.1:n.398C>T
ENST00000698434.1:n.423C>T
ENST00000244137.12:c.936C>T MANE Select	ENSP00000244137.5:p.Ser312=
ENST00000588328.6:c.925C>T
ENST00000590731.6:n.611C>T
ENST00000651901.1:c.932C>T
ENST00000244137.11:c.936C>T	ENSP00000244137.5:p.Ser312=
ENST00000397032.8:c.813C>T	ENSP00000380226.3:p.Ser271=
ENST00000436370.7:c.744C>T	ENSP00000391890.2:p.Ser248=
ENST00000588328.5:c.427C>T
NM_000285.3:c.936C>T	NP_000276.2:p.Ser312=
NM_001166056.1:c.813C>T	NP_001159528.1:p.Ser271=
NM_001166057.1:c.744C>T	NP_001159529.1:p.Ser248=
NM_000285.4:c.936C>T MANE Select	NP_000276.2:p.Ser312=
NM_001166056.2:c.813C>T	NP_001159528.1:p.Ser271=
NM_001166057.2:c.744C>T	NP_001159529.1:p.Ser248=