Canonical Allele Identifier: CA1319033814

Gene: PGAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.196912861T= , CM000664.2:g.196912861T=	GRCh38
NC_000002.11:g.197777585T= , CM000664.1:g.197777585T=	GRCh37
NC_000002.10:g.197485830T=	NCBI36
NG_046780.1:g.19135A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000354764.9:c.649+21A= MANE Select	ENSP00000346809.3:n.649+21A=
ENST00000354764.8:c.649+21A=	ENSP00000346809.3:n.649+21A=
ENST00000374738.3:c.147+13609A=	ENSP00000363870.3:n.147+13609A=
ENST00000409188.5:c.523+21A=	ENSP00000386802.1:n.523+21A=
ENST00000409475.5:c.649+21A=	ENSP00000387028.1:n.649+21A=
ENST00000423035.5:c.*580+21A=	ENSP00000415405.1:n.*580+21A=
ENST00000470179.5:n.271+13609A=
ENST00000485830.1:n.793+21A=
NM_024989.3:c.649+21A=	NP_079265.2:n.649+21A=
XM_011511878.1:c.649+21A=	XP_011510180.1:n.649+21A=
XM_011511879.1:c.127+21A=	XP_011510181.1:n.127+21A=
XM_011511880.1:c.649+21A=	XP_011510182.1:n.649+21A=
NM_001321099.1:c.127+21A=	NP_001308028.1:n.127+21A=
NM_001321100.1:c.-463+21A=	NP_001308029.1:n.-463+21A=
XM_017004992.1:c.127+21A=	XP_016860481.1:n.127+21A=
XM_017004993.1:c.127+21A=	XP_016860482.1:n.127+21A=
XM_017004994.1:c.-463+21A=	XP_016860483.1:n.-463+21A=
XM_024453156.1:c.-509+21A=	XP_024308924.1:n.-509+21A=
XR_001738959.1:n.1028+21A=
XR_001738960.1:n.1028+21A=
NM_024989.4:c.649+21A= MANE Select	NP_079265.2:n.649+21A=
NM_001321099.2:c.127+21A=	NP_001308028.1:n.127+21A=
NM_001321100.2:c.-463+21A=	NP_001308029.1:n.-463+21A=