Canonical Allele Identifier: CA399317622

Gene: PGAP3

Linked Data

• gnomAD v4: 17-39672289-A-C
• MyVariant Identifiers: chr17:g.37828542A>C (hg19) ; chr17:g.39672289A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39672289A>C , CM000679.2:g.39672289A>C	GRCh38
NC_000017.10:g.37828542A>C , CM000679.1:g.37828542A>C	GRCh37
NC_000017.9:g.35082068A>C	NCBI36
NG_034125.1:g.20782T>G
NG_042278.1:g.9309A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300658.9:c.*514T>G MANE Select	ENSP00000300658.4:n.*514T>G
ENST00000300658.8:c.*514T>G	ENSP00000300658.4:n.*514T>G
ENST00000309862.10:n.1862T>G
ENST00000378011.8:c.*514T>G	ENSP00000367250.4:n.*514T>G
ENST00000579146.5:c.*563T>G	ENSP00000463234.1:n.*563T>G
ENST00000614824.4:c.*514T>G	ENSP00000480165.1:n.*514T>G
ENST00000619169.4:c.403T>G	ENSP00000478028.1:p.Leu135Val
NM_001291726.1:c.*514T>G	NP_001278655.1:n.*514T>G
NM_001291728.1:c.*514T>G	NP_001278657.1:n.*514T>G
NM_001291730.1:c.*514T>G	NP_001278659.1:n.*514T>G
NM_001291732.1:c.*514T>G	NP_001278661.1:n.*514T>G
NM_001291733.1:c.*563T>G	NP_001278662.1:n.*563T>G
NM_033419.4:c.*514T>G	NP_219487.3:n.*514T>G
XM_011525481.1:c.*514T>G	XP_011523783.1:n.*514T>G
XM_011525480.2:c.*546T>G	XP_011523782.1:n.*546T>G
XM_011525481.2:c.*514T>G	XP_011523783.1:n.*514T>G
XR_002958086.1:n.2004T>G
NM_033419.5:c.*514T>G MANE Select	NP_219487.3:n.*514T>G
NM_001291726.2:c.*514T>G	NP_001278655.1:n.*514T>G
NM_001291728.2:c.*514T>G	NP_001278657.1:n.*514T>G
NM_001291730.2:c.*514T>G	NP_001278659.1:n.*514T>G
NM_001291732.2:c.*514T>G	NP_001278661.1:n.*514T>G
NM_001291733.2:c.*563T>G	NP_001278662.1:n.*563T>G