Canonical Allele Identifier: CA1319034001

Gene: PGAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.196912956T= , CM000664.2:g.196912956T=	GRCh38
NC_000002.11:g.197777680T= , CM000664.1:g.197777680T=	GRCh37
NC_000002.10:g.197485925T=	NCBI36
NG_046780.1:g.19040A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354764.9:c.575A= MANE Select	ENSP00000346809.3:p.Asp192=
ENST00000354764.8:c.575A=	ENSP00000346809.3:p.Asp192=
ENST00000374738.3:c.147+13514A=	ENSP00000363870.3:n.147+13514A=
ENST00000409188.5:c.449A=	ENSP00000386802.1:p.Asp150=
ENST00000409475.5:c.575A=	ENSP00000387028.1:p.Asp192=
ENST00000423035.5:c.*506A=	ENSP00000415405.1:n.*506A=
ENST00000470179.5:n.271+13514A=
ENST00000485830.1:n.719A=
NM_024989.3:c.575A=	NP_079265.2:p.Asp192=
XM_011511878.1:c.575A=	XP_011510180.1:p.Asp192=
XM_011511879.1:c.53A=	XP_011510181.1:p.Asp18=
XM_011511880.1:c.575A=	XP_011510182.1:p.Asp192=
NM_001321099.1:c.53A=	NP_001308028.1:p.Asp18=
NM_001321100.1:c.-537A=	NP_001308029.1:n.-537A=
XM_017004992.1:c.53A=	XP_016860481.1:p.Asp18=
XM_017004993.1:c.53A=	XP_016860482.1:p.Asp18=
XM_017004994.1:c.-537A=	XP_016860483.1:n.-537A=
XM_024453156.1:c.-583A=	XP_024308924.1:n.-583A=
XR_001738959.1:n.954A=
XR_001738960.1:n.954A=
NM_024989.4:c.575A= MANE Select	NP_079265.2:p.Asp192=
NM_001321099.2:c.53A=	NP_001308028.1:p.Asp18=
NM_001321100.2:c.-537A=	NP_001308029.1:n.-537A=