Canonical Allele Identifier: CA2561832428

Gene: HPGD

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.174493107_174493108insCA , CM000666.2:g.174493107_174493108insCA	GRCh38
NC_000004.11:g.175414258_175414259insCA , CM000666.1:g.175414258_175414259insCA	GRCh37
NC_000004.10:g.175650833_175650834insCA	NCBI36
NG_011689.1:g.34534_34535insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296522.11:c.662+43_662+44insTG MANE Select	ENSP00000296522.6:n.662+43_662+44insTG
ENST00000296521.11:c.499-1014_499-1013insTG	ENSP00000296521.7:n.499-1014_499-1013insTG
ENST00000296522.10:c.662+43_662+44insTG	ENSP00000296522.6:n.662+43_662+44insTG
ENST00000422112.6:c.458+43_458+44insTG	ENSP00000398720.2:n.458+43_458+44insTG
ENST00000508330.5:c.*291+43_*291+44insTG	ENSP00000425741.1:n.*291+43_*291+44insTG
ENST00000509512.1:n.311+43_311+44insTG
ENST00000510835.5:c.*424+43_*424+44insTG	ENSP00000427699.1:n.*424+43_*424+44insTG
ENST00000510901.5:c.299+43_299+44insTG	ENSP00000422418.1:n.299+43_299+44insTG
ENST00000511499.5:n.446+43_446+44insTG
ENST00000541923.5:c.299+43_299+44insTG	ENSP00000438017.1:n.299+43_299+44insTG
ENST00000542498.5:c.422-1014_422-1013insTG	ENSP00000443644.1:n.422-1014_422-1013insTG
NM_000860.5:c.662+43_662+44insTG	NP_000851.2:n.662+43_662+44insTG
NM_001145816.2:c.499-1014_499-1013insTG	NP_001139288.1:n.499-1014_499-1013insTG
NM_001256301.1:c.299+43_299+44insTG	NP_001243230.1:n.299+43_299+44insTG
NM_001256305.1:c.422-1014_422-1013insTG	NP_001243234.1:n.422-1014_422-1013insTG
NM_001256306.1:c.458+43_458+44insTG	NP_001243235.1:n.458+43_458+44insTG
NM_001256307.1:c.299+43_299+44insTG	NP_001243236.1:n.299+43_299+44insTG
NM_000860.6:c.662+43_662+44insTG MANE Select	NP_000851.2:n.662+43_662+44insTG
NM_001145816.3:c.499-1014_499-1013insTG	NP_001139288.1:n.499-1014_499-1013insTG
NM_001256305.2:c.422-1014_422-1013insTG	NP_001243234.1:n.422-1014_422-1013insTG
NM_001256306.2:c.458+43_458+44insTG	NP_001243235.1:n.458+43_458+44insTG
NM_001256307.2:c.299+43_299+44insTG	NP_001243236.1:n.299+43_299+44insTG