Canonical Allele Identifier: CA9367109

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34377851C>G , CM000681.2:g.34377851C>G	GRCh38
NC_000019.9:g.34868756C>G , CM000681.1:g.34868756C>G	GRCh37
NC_000019.8:g.39560596C>G	NCBI36
NG_012838.2:g.18112C>G
NG_012838.3:g.23260C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.603C>G MANE Select	ENSP00000348877.3:p.Pro201=
ENST00000415930.8:c.720C>G	ENSP00000405573.3:p.Pro240=
ENST00000586425.2:c.491C>G
ENST00000588991.7:c.636C>G	ENSP00000465858.3:p.Pro212=
ENST00000589399.6:c.403-1083C>G	ENSP00000468201.2:n.403-1083C>G
ENST00000643067.1:n.1113C>G
ENST00000647446.1:c.603C>G	ENSP00000495129.1:p.Pro201=
ENST00000356487.9:c.603C>G	ENSP00000348877.3:p.Pro201=
ENST00000415930.7:c.636C>G	ENSP00000405573.2:p.Pro212=
ENST00000586425.1:c.603C>G	ENSP00000467670.2:p.Pro201=
ENST00000588991.6:c.648C>G	ENSP00000465858.2:p.Pro216=
ENST00000591204.5:c.483C>G	ENSP00000466851.2:p.Pro161=
NM_000175.3:c.603C>G	NP_000166.2:p.Pro201=
NM_001184722.1:c.636C>G	NP_001171651.1:p.Pro212=
NM_001289789.1:c.720C>G	NP_001276718.1:p.Pro240=
NM_001289790.1:c.519C>G	NP_001276719.1:p.Pro173=
XM_005258764.1:c.603C>G	XP_005258821.1:p.Pro201=
XM_006723148.1:c.603C>G	XP_006723211.1:p.Pro201=
XM_011526754.1:c.720C>G	XP_011525056.1:p.Pro240=
XM_011526755.1:c.720C>G	XP_011525057.1:p.Pro240=
NM_000175.5:c.603C>G MANE Select	NP_000166.2:p.Pro201=
NM_001289790.2:c.519C>G	NP_001276719.1:p.Pro173=
NM_001329909.1:c.603C>G	NP_001316838.1:p.Pro201=
NM_001329910.1:c.603C>G	NP_001316839.1:p.Pro201=
NM_001329911.1:c.603C>G	NP_001316840.1:p.Pro201=
XM_011526754.3:c.720C>G	XP_011525056.1:p.Pro240=
NM_001289790.3:c.519C>G	NP_001276719.1:p.Pro173=
NM_001329911.2:c.603C>G	NP_001316840.1:p.Pro201=