Canonical Allele Identifier: CA512936496

Gene: PRODH DGCR6

Linked Data

• MyVariant Identifiers: chr22:g.18900733G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913220G>C , CM000684.2:g.18913220G>C	GRCh38
NC_000022.10:g.18900733G>C , CM000684.1:g.18900733G>C	GRCh37
NC_000022.9:g.17280733G>C	NCBI36
NG_008226.2:g.28334C>G
NG_009052.1:g.11998G>C
NG_008226.3:g.28334C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1758C>G (PRODH) MANE Select	ENSP00000349577.6:p.Leu586=
ENST00000638240.1:c.513+2192G>C	ENSP00000492446.1:n.513+2192G>C
ENST00000313755.9:n.2523C>G (PRODH)
ENST00000334029.6:c.1434C>G (PRODH)	ENSP00000334726.2:p.Leu478=
ENST00000357068.10:c.1758C>G (PRODH)	ENSP00000349577.6:p.Leu586=
ENST00000420436.5:c.1434C>G (PRODH)	ENSP00000410805.1:p.Leu478=
ENST00000429300.5:n.2129C>G (PRODH)
ENST00000482858.5:n.4238C>G (PRODH)
ENST00000483718.5:c.*1862G>C (DGCR6)	ENSP00000467483.1:n.*1862G>C
ENST00000491604.5:n.2667C>G (PRODH)
ENST00000610940.4:c.1758C>G (PRODH)	ENSP00000480347.1:p.Leu586=
NM_001195226.1:c.1434C>G (PRODH)	NP_001182155.1:p.Leu478=
NM_016335.4:c.1758C>G (PRODH)	NP_057419.4:p.Leu586=
XM_011530278.1:c.1185C>G (PRODH)	XP_011528580.1:p.Leu395=
XM_011530279.1:c.978C>G (PRODH)	XP_011528581.1:p.Leu326=
XR_937876.1:n.1825C>G (PRODH)
NM_005675.5:c.*1531G>C (DGCR6)	NP_005666.2:n.*1531G>C
NM_001195226.2:c.1434C>G (PRODH)	NP_001182155.2:p.Leu478=
NM_016335.5:c.1758C>G (PRODH)	NP_057419.5:p.Leu586=
NM_016335.6:c.1758C>G (PRODH) MANE Select	NP_057419.5:p.Leu586=