Canonical Allele Identifier: CA506687136

Gene: PEPD

Linked Data

• MyVariant Identifiers: chr19:g.33954914G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33464008G>A , CM000681.2:g.33464008G>A	GRCh38
NC_000019.9:g.33954914G>A , CM000681.1:g.33954914G>A	GRCh37
NC_000019.8:g.38646754G>A	NCBI36
NG_013358.1:g.62886C>T
NG_013358.2:g.62886C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000588328.7:c.603C>T	ENSP00000468516.4:p.Ile201=
ENST00000651646.2:c.603C>T	ENSP00000498950.2:p.Ile201=
ENST00000651901.2:c.603C>T	ENSP00000498922.2:p.Ile201=
ENST00000698359.1:c.558C>T	ENSP00000513682.1:p.Ile186=
ENST00000698360.1:c.603C>T	ENSP00000513683.1:p.Ile201=
ENST00000698361.1:c.603C>T	ENSP00000513684.1:p.Ile201=
ENST00000698362.1:c.603C>T	ENSP00000513685.1:p.Ile201=
ENST00000698363.1:n.666C>T
ENST00000698364.1:n.666C>T
ENST00000698365.1:n.666C>T
ENST00000698426.1:c.282C>T	ENSP00000513713.1:p.Ile94=
ENST00000698427.1:c.645C>T	ENSP00000513714.1:p.Ile215=
ENST00000698428.1:c.282C>T	ENSP00000513715.1:p.Ile94=
ENST00000698430.1:c.853C>T
ENST00000698431.1:c.340C>T	ENSP00000513717.1:n.340C>T
ENST00000698432.1:c.412C>T
ENST00000698435.1:c.291C>T	ENSP00000513719.1:p.Ile97=
ENST00000698436.1:c.*215C>T	ENSP00000513720.1:n.*215C>T
ENST00000698437.1:n.586C>T
ENST00000698438.1:n.585C>T
ENST00000698439.1:c.460C>T	ENSP00000513721.1:n.460C>T
ENST00000244137.12:c.603C>T MANE Select	ENSP00000244137.5:p.Ile201=
ENST00000588328.6:c.592C>T
ENST00000590731.6:n.278C>T
ENST00000651646.1:c.601C>T
ENST00000651901.1:c.599C>T
ENST00000244137.11:c.603C>T	ENSP00000244137.5:p.Ile201=
ENST00000397032.8:c.548+14038C>T	ENSP00000380226.3:n.548+14038C>T
ENST00000436370.7:c.411C>T	ENSP00000391890.2:p.Ile137=
ENST00000588328.5:c.94C>T
ENST00000588719.5:n.238C>T
ENST00000590408.1:c.321C>T
ENST00000590731.5:n.278C>T
ENST00000590755.6:c.430C>T	ENSP00000476667.1:n.430C>T
ENST00000593163.5:n.768C>T
ENST00000609145.5:c.36C>T	ENSP00000476514.1:p.Ile12=
NM_000285.3:c.603C>T	NP_000276.2:p.Ile201=
NM_001166056.1:c.548+14038C>T	NP_001159528.1:n.548+14038C>T
NM_001166057.1:c.411C>T	NP_001159529.1:p.Ile137=
NM_000285.4:c.603C>T MANE Select	NP_000276.2:p.Ile201=
NM_001166056.2:c.548+14038C>T	NP_001159528.1:n.548+14038C>T
NM_001166057.2:c.411C>T	NP_001159529.1:p.Ile137=