Canonical Allele Identifier: CA350179474

Gene: PGAP1

Linked Data

• MyVariant Identifiers: chr2:g.197777675T>C (hg19) ; chr2:g.196912951T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.196912951T>C , CM000664.2:g.196912951T>C	GRCh38
NC_000002.11:g.197777675T>C , CM000664.1:g.197777675T>C	GRCh37
NC_000002.10:g.197485920T>C	NCBI36
NG_046780.1:g.19045A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354764.9:c.580A>G MANE Select	ENSP00000346809.3:p.Ile194Val
ENST00000354764.8:c.580A>G	ENSP00000346809.3:p.Ile194Val
ENST00000374738.3:c.147+13519A>G	ENSP00000363870.3:n.147+13519A>G
ENST00000409188.5:c.454A>G	ENSP00000386802.1:p.Ile152Val
ENST00000409475.5:c.580A>G	ENSP00000387028.1:p.Ile194Val
ENST00000423035.5:c.*511A>G	ENSP00000415405.1:n.*511A>G
ENST00000470179.5:n.271+13519A>G
ENST00000485830.1:n.724A>G
NM_024989.3:c.580A>G	NP_079265.2:p.Ile194Val
XM_011511878.1:c.580A>G	XP_011510180.1:p.Ile194Val
XM_011511879.1:c.58A>G	XP_011510181.1:p.Ile20Val
XM_011511880.1:c.580A>G	XP_011510182.1:p.Ile194Val
NM_001321099.1:c.58A>G	NP_001308028.1:p.Ile20Val
NM_001321100.1:c.-532A>G	NP_001308029.1:n.-532A>G
XM_017004992.1:c.58A>G	XP_016860481.1:p.Ile20Val
XM_017004993.1:c.58A>G	XP_016860482.1:p.Ile20Val
XM_017004994.1:c.-532A>G	XP_016860483.1:n.-532A>G
XM_024453156.1:c.-578A>G	XP_024308924.1:n.-578A>G
XR_001738959.1:n.959A>G
XR_001738960.1:n.959A>G
NM_024989.4:c.580A>G MANE Select	NP_079265.2:p.Ile194Val
NM_001321099.2:c.58A>G	NP_001308028.1:p.Ile20Val
NM_001321100.2:c.-532A>G	NP_001308029.1:n.-532A>G