Canonical Allele Identifier: CA405246088

Gene: GPI

Linked Data

• MyVariant Identifiers: chr19:g.34890500A>T (hg19) ; chr19:g.34399595A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399595A>T , CM000681.2:g.34399595A>T	GRCh38
NC_000019.9:g.34890500A>T , CM000681.1:g.34890500A>T	GRCh37
NC_000019.8:g.39582340A>T	NCBI36
NG_012838.2:g.39856A>T
NG_012838.3:g.45004A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1438A>T MANE Select	ENSP00000348877.3:p.Thr480Ser
ENST00000415930.8:c.1555A>T	ENSP00000405573.3:p.Thr519Ser
ENST00000586425.2:c.1158-141A>T
ENST00000588991.7:c.1471A>T	ENSP00000465858.3:p.Thr491Ser
ENST00000643067.1:n.2483A>T
ENST00000647446.1:c.*489A>T	ENSP00000495129.1:n.*489A>T
ENST00000356487.9:c.1438A>T	ENSP00000348877.3:p.Thr480Ser
ENST00000415930.7:c.1471A>T	ENSP00000405573.2:p.Thr491Ser
ENST00000586077.1:n.2313A>T
ENST00000586392.1:n.1176A>T
ENST00000586425.1:c.1398+260A>T	ENSP00000467670.2:n.1398+260A>T
ENST00000588991.6:c.1483A>T	ENSP00000465858.2:p.Thr495Ser
ENST00000592740.5:c.193+2938A>T
NM_000175.3:c.1438A>T	NP_000166.2:p.Thr480Ser
NM_001184722.1:c.1471A>T	NP_001171651.1:p.Thr491Ser
NM_001289789.1:c.1555A>T	NP_001276718.1:p.Thr519Ser
NM_001289790.1:c.1354A>T	NP_001276719.1:p.Thr452Ser
XM_005258764.1:c.1438A>T	XP_005258821.1:p.Thr480Ser
XM_006723148.1:c.1438A>T	XP_006723211.1:p.Thr480Ser
XM_011526754.1:c.1555A>T	XP_011525056.1:p.Thr519Ser
NM_000175.5:c.1438A>T MANE Select	NP_000166.2:p.Thr480Ser
NM_001289790.2:c.1354A>T	NP_001276719.1:p.Thr452Ser
NM_001329909.1:c.1438A>T	NP_001316838.1:p.Thr480Ser
NM_001329910.1:c.1438A>T	NP_001316839.1:p.Thr480Ser
NM_001329911.1:c.1411A>T	NP_001316840.1:p.Thr471Ser
XM_011526754.3:c.1555A>T	XP_011525056.1:p.Thr519Ser
NM_001289790.3:c.1354A>T	NP_001276719.1:p.Thr452Ser
NM_001329911.2:c.1411A>T	NP_001316840.1:p.Thr471Ser