Canonical Allele Identifier: CA405246238

Gene: GPI

Linked Data

• MyVariant Identifiers: chr19:g.34890525G>T (hg19) ; chr19:g.34399620G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399620G>T , CM000681.2:g.34399620G>T	GRCh38
NC_000019.9:g.34890525G>T , CM000681.1:g.34890525G>T	GRCh37
NC_000019.8:g.39582365G>T	NCBI36
NG_012838.2:g.39881G>T
NG_012838.3:g.45029G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1463G>T MANE Select	ENSP00000348877.3:p.Gly488Val
ENST00000415930.8:c.1580G>T	ENSP00000405573.3:p.Gly527Val
ENST00000586425.2:c.1158-116G>T
ENST00000588991.7:c.1496G>T	ENSP00000465858.3:p.Gly499Val
ENST00000643067.1:n.2508G>T
ENST00000647446.1:c.*514G>T	ENSP00000495129.1:n.*514G>T
ENST00000356487.9:c.1463G>T	ENSP00000348877.3:p.Gly488Val
ENST00000415930.7:c.1496G>T	ENSP00000405573.2:p.Gly499Val
ENST00000586077.1:n.2338G>T
ENST00000586392.1:n.1201G>T
ENST00000586425.1:c.1399-281G>T	ENSP00000467670.2:n.1399-281G>T
ENST00000588991.6:c.1508G>T	ENSP00000465858.2:p.Gly503Val
ENST00000592740.5:c.193+2963G>T
NM_000175.3:c.1463G>T	NP_000166.2:p.Gly488Val
NM_001184722.1:c.1496G>T	NP_001171651.1:p.Gly499Val
NM_001289789.1:c.1580G>T	NP_001276718.1:p.Gly527Val
NM_001289790.1:c.1379G>T	NP_001276719.1:p.Gly460Val
XM_005258764.1:c.1463G>T	XP_005258821.1:p.Gly488Val
XM_006723148.1:c.1463G>T	XP_006723211.1:p.Gly488Val
XM_011526754.1:c.1580G>T	XP_011525056.1:p.Gly527Val
NM_000175.5:c.1463G>T MANE Select	NP_000166.2:p.Gly488Val
NM_001289790.2:c.1379G>T	NP_001276719.1:p.Gly460Val
NM_001329909.1:c.1463G>T	NP_001316838.1:p.Gly488Val
NM_001329910.1:c.1463G>T	NP_001316839.1:p.Gly488Val
NM_001329911.1:c.1436G>T	NP_001316840.1:p.Gly479Val
XM_011526754.3:c.1580G>T	XP_011525056.1:p.Gly527Val
NM_001289790.3:c.1379G>T	NP_001276719.1:p.Gly460Val
NM_001329911.2:c.1436G>T	NP_001316840.1:p.Gly479Val