Canonical Allele Identifier: CA399315173

Gene: PGAP3

Linked Data

• dbSNP Id: rs1597810362
• MyVariant Identifiers: chr17:g.37828299A>T (hg19) ; chr17:g.39672046A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39672046A>T , CM000679.2:g.39672046A>T	GRCh38
NC_000017.10:g.37828299A>T , CM000679.1:g.37828299A>T	GRCh37
NC_000017.9:g.35081825A>T	NCBI36
NG_034125.1:g.21025T>A
NG_042278.1:g.9066A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300658.9:c.*757T>A MANE Select	ENSP00000300658.4:n.*757T>A
ENST00000300658.8:c.*757T>A	ENSP00000300658.4:n.*757T>A
ENST00000309862.10:n.2105T>A
ENST00000378011.8:c.*757T>A	ENSP00000367250.4:n.*757T>A
ENST00000579146.5:c.*806T>A	ENSP00000463234.1:n.*806T>A
ENST00000614824.4:c.*757T>A	ENSP00000480165.1:n.*757T>A
ENST00000619169.4:c.646T>A	ENSP00000478028.1:p.Cys216Ser
NM_001291726.1:c.*757T>A	NP_001278655.1:n.*757T>A
NM_001291728.1:c.*757T>A	NP_001278657.1:n.*757T>A
NM_001291730.1:c.*757T>A	NP_001278659.1:n.*757T>A
NM_001291732.1:c.*757T>A	NP_001278661.1:n.*757T>A
NM_001291733.1:c.*806T>A	NP_001278662.1:n.*806T>A
NM_033419.4:c.*757T>A	NP_219487.3:n.*757T>A
XM_011525480.2:c.*789T>A	XP_011523782.1:n.*789T>A
XM_011525481.2:c.*757T>A	XP_011523783.1:n.*757T>A
XR_002958086.1:n.2247T>A
NM_033419.5:c.*757T>A MANE Select	NP_219487.3:n.*757T>A
NM_001291726.2:c.*757T>A	NP_001278655.1:n.*757T>A
NM_001291728.2:c.*757T>A	NP_001278657.1:n.*757T>A
NM_001291730.2:c.*757T>A	NP_001278659.1:n.*757T>A
NM_001291732.2:c.*757T>A	NP_001278661.1:n.*757T>A
NM_001291733.2:c.*806T>A	NP_001278662.1:n.*806T>A