Canonical Allele Identifier: CA371694427

Gene: PDP1

Linked Data

• gnomAD v4: 8-93922903-G-T
• MyVariant Identifiers: chr8:g.94935131G>T (hg19) ; chr8:g.93922903G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93922903G>T , CM000670.2:g.93922903G>T	GRCh38
NC_000008.10:g.94935131G>T , CM000670.1:g.94935131G>T	GRCh37
NC_000008.9:g.95004307G>T	NCBI36
NG_012233.1:g.10970G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297598.5:c.844G>T MANE Select	ENSP00000297598.4:p.Val282Phe
ENST00000297598.4:c.844G>T	ENSP00000297598.4:p.Val282Phe
ENST00000396200.3:c.919G>T	ENSP00000379503.3:p.Val307Phe
ENST00000517764.1:c.844G>T	ENSP00000430380.1:p.Val282Phe
ENST00000520728.5:c.844G>T	ENSP00000428317.1:p.Val282Phe
NM_001161779.1:c.919G>T	NP_001155251.1:p.Val307Phe
NM_001161780.1:c.919G>T	NP_001155252.1:p.Val307Phe
NM_001161781.1:c.844G>T	NP_001155253.1:p.Val282Phe
NM_018444.3:c.844G>T	NP_060914.2:p.Val282Phe
XM_011517135.1:c.898G>T	XP_011515437.1:p.Val300Phe
XM_011517136.1:c.844G>T	XP_011515438.1:p.Val282Phe
XM_011517137.1:c.844G>T	XP_011515439.1:p.Val282Phe
XM_011517135.2:c.898G>T	XP_011515437.1:p.Val300Phe
XM_011517136.2:c.844G>T	XP_011515438.1:p.Val282Phe
XM_017013588.1:c.1006G>T	XP_016869077.1:p.Val336Phe
NM_018444.4:c.844G>T MANE Select	NP_060914.2:p.Val282Phe
NM_001161780.2:c.919G>T	NP_001155252.1:p.Val307Phe
NM_001161781.2:c.844G>T	NP_001155253.1:p.Val282Phe
NM_001161779.2:c.919G>T	NP_001155251.1:p.Val307Phe