Canonical Allele Identifier: CA371694483

Gene: PDP1

Linked Data

• MyVariant Identifiers: chr8:g.94935149A>C (hg19) ; chr8:g.93922921A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93922921A>C , CM000670.2:g.93922921A>C	GRCh38
NC_000008.10:g.94935149A>C , CM000670.1:g.94935149A>C	GRCh37
NC_000008.9:g.95004325A>C	NCBI36
NG_012233.1:g.10988A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297598.5:c.862A>C MANE Select	ENSP00000297598.4:p.Asn288His
ENST00000297598.4:c.862A>C	ENSP00000297598.4:p.Asn288His
ENST00000396200.3:c.937A>C	ENSP00000379503.3:p.Asn313His
ENST00000517764.1:c.862A>C	ENSP00000430380.1:p.Asn288His
ENST00000520728.5:c.862A>C	ENSP00000428317.1:p.Asn288His
NM_001161779.1:c.937A>C	NP_001155251.1:p.Asn313His
NM_001161780.1:c.937A>C	NP_001155252.1:p.Asn313His
NM_001161781.1:c.862A>C	NP_001155253.1:p.Asn288His
NM_018444.3:c.862A>C	NP_060914.2:p.Asn288His
XM_011517135.1:c.916A>C	XP_011515437.1:p.Asn306His
XM_011517136.1:c.862A>C	XP_011515438.1:p.Asn288His
XM_011517137.1:c.862A>C	XP_011515439.1:p.Asn288His
XM_011517135.2:c.916A>C	XP_011515437.1:p.Asn306His
XM_011517136.2:c.862A>C	XP_011515438.1:p.Asn288His
XM_017013588.1:c.1024A>C	XP_016869077.1:p.Asn342His
NM_018444.4:c.862A>C MANE Select	NP_060914.2:p.Asn288His
NM_001161780.2:c.937A>C	NP_001155252.1:p.Asn313His
NM_001161781.2:c.862A>C	NP_001155253.1:p.Asn288His
NM_001161779.2:c.937A>C	NP_001155251.1:p.Asn313His