Canonical Allele Identifier: CA9367153

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34378972G>A , CM000681.2:g.34378972G>A	GRCh38
NC_000019.9:g.34869877G>A , CM000681.1:g.34869877G>A	GRCh37
NC_000019.8:g.39561717G>A	NCBI36
NG_012838.2:g.19233G>A
NG_012838.3:g.24381G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.672G>A MANE Select	ENSP00000348877.3:p.Thr224=
ENST00000415930.8:c.789G>A	ENSP00000405573.3:p.Thr263=
ENST00000586425.2:c.560G>A
ENST00000588991.7:c.705G>A	ENSP00000465858.3:p.Thr235=
ENST00000589399.6:c.441G>A	ENSP00000468201.2:p.Thr147=
ENST00000643067.1:n.1182G>A
ENST00000647446.1:c.672G>A	ENSP00000495129.1:p.Thr224=
ENST00000356487.9:c.672G>A	ENSP00000348877.3:p.Thr224=
ENST00000415930.7:c.705G>A	ENSP00000405573.2:p.Thr235=
ENST00000586425.1:c.672G>A	ENSP00000467670.2:p.Thr224=
ENST00000588991.6:c.717G>A	ENSP00000465858.2:p.Thr239=
NM_000175.3:c.672G>A	NP_000166.2:p.Thr224=
NM_001184722.1:c.705G>A	NP_001171651.1:p.Thr235=
NM_001289789.1:c.789G>A	NP_001276718.1:p.Thr263=
NM_001289790.1:c.588G>A	NP_001276719.1:p.Thr196=
XM_005258764.1:c.672G>A	XP_005258821.1:p.Thr224=
XM_006723148.1:c.672G>A	XP_006723211.1:p.Thr224=
XM_011526754.1:c.789G>A	XP_011525056.1:p.Thr263=
XM_011526755.1:c.789G>A	XP_011525057.1:p.Thr263=
NM_000175.5:c.672G>A MANE Select	NP_000166.2:p.Thr224=
NM_001289790.2:c.588G>A	NP_001276719.1:p.Thr196=
NM_001329909.1:c.672G>A	NP_001316838.1:p.Thr224=
NM_001329910.1:c.672G>A	NP_001316839.1:p.Thr224=
NM_001329911.1:c.672G>A	NP_001316840.1:p.Thr224=
XM_011526754.3:c.789G>A	XP_011525056.1:p.Thr263=
NM_001289790.3:c.588G>A	NP_001276719.1:p.Thr196=
NM_001329911.2:c.672G>A	NP_001316840.1:p.Thr224=