Canonical Allele Identifier: CA405224777

Gene: PEPD

Linked Data

• gnomAD v4: 19-33401858-A-C
• MyVariant Identifiers: chr19:g.33892764A>C (hg19) ; chr19:g.33401858A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33401858A>C , CM000681.2:g.33401858A>C	GRCh38
NC_000019.9:g.33892764A>C , CM000681.1:g.33892764A>C	GRCh37
NC_000019.8:g.38584604A>C	NCBI36
NG_013358.1:g.125036T>G
NG_013358.2:g.125036T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000588328.7:c.830T>G	ENSP00000468516.4:p.Met277Arg
ENST00000651901.2:c.830T>G	ENSP00000498922.2:p.Met277Arg
ENST00000698359.1:c.785T>G	ENSP00000513682.1:p.Met262Arg
ENST00000698360.1:c.881T>G	ENSP00000513683.1:p.Met294Arg
ENST00000698361.1:c.830T>G	ENSP00000513684.1:p.Met277Arg
ENST00000698362.1:c.830T>G	ENSP00000513685.1:p.Met277Arg
ENST00000698363.1:n.893T>G
ENST00000698364.1:n.893T>G
ENST00000698365.1:n.893T>G
ENST00000698426.1:c.509T>G	ENSP00000513713.1:p.Met170Arg
ENST00000698427.1:c.872T>G	ENSP00000513714.1:p.Met291Arg
ENST00000698428.1:c.509T>G	ENSP00000513715.1:p.Met170Arg
ENST00000698429.1:n.713T>G
ENST00000698430.1:c.1080T>G
ENST00000698431.1:c.567T>G	ENSP00000513717.1:n.567T>G
ENST00000698432.1:c.639T>G
ENST00000698433.1:n.292T>G
ENST00000698434.1:n.317T>G
ENST00000698435.1:c.518T>G	ENSP00000513719.1:p.Met173Arg
ENST00000244137.12:c.830T>G MANE Select	ENSP00000244137.5:p.Met277Arg
ENST00000588328.6:c.819T>G
ENST00000590731.6:n.505T>G
ENST00000651901.1:c.826T>G
ENST00000244137.11:c.830T>G	ENSP00000244137.5:p.Met277Arg
ENST00000397032.8:c.707T>G	ENSP00000380226.3:p.Met236Arg
ENST00000436370.7:c.638T>G	ENSP00000391890.2:p.Met213Arg
ENST00000588328.5:c.321T>G
ENST00000588719.5:n.465T>G
ENST00000590731.5:n.505T>G
ENST00000593163.5:n.995T>G
ENST00000609145.5:c.263T>G	ENSP00000476514.1:p.Met88Arg
NM_000285.3:c.830T>G	NP_000276.2:p.Met277Arg
NM_001166056.1:c.707T>G	NP_001159528.1:p.Met236Arg
NM_001166057.1:c.638T>G	NP_001159529.1:p.Met213Arg
NM_000285.4:c.830T>G MANE Select	NP_000276.2:p.Met277Arg
NM_001166056.2:c.707T>G	NP_001159528.1:p.Met236Arg
NM_001166057.2:c.638T>G	NP_001159529.1:p.Met213Arg