Canonical Allele Identifier: CA506999829

Gene: GPI

Linked Data

• gnomAD v4: 19-34400000-C-T
• MyVariant Identifiers: chr19:g.34890905C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34400000C>T , CM000681.2:g.34400000C>T	GRCh38
NC_000019.9:g.34890905C>T , CM000681.1:g.34890905C>T	GRCh37
NC_000019.8:g.39582745C>T	NCBI36
NG_012838.2:g.40261C>T
NG_012838.3:g.45409C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1641C>T MANE Select	ENSP00000348877.3:p.Asn547=
ENST00000415930.8:c.1758C>T	ENSP00000405573.3:p.Asn586=
ENST00000586425.2:c.1307C>T
ENST00000588991.7:c.1674C>T	ENSP00000465858.3:p.Asn558=
ENST00000643067.1:n.2686C>T
ENST00000647446.1:c.*692C>T	ENSP00000495129.1:n.*692C>T
ENST00000356487.9:c.1641C>T	ENSP00000348877.3:p.Asn547=
ENST00000415930.7:c.1674C>T	ENSP00000405573.2:p.Asn558=
ENST00000586077.1:n.2718C>T
ENST00000586392.1:n.1379C>T
ENST00000586425.1:c.*73C>T	ENSP00000467670.2:n.*73C>T
ENST00000588991.6:c.1686C>T	ENSP00000465858.2:p.Asn562=
ENST00000592740.5:c.193+3343C>T
NM_000175.3:c.1641C>T	NP_000166.2:p.Asn547=
NM_001184722.1:c.1674C>T	NP_001171651.1:p.Asn558=
NM_001289789.1:c.1758C>T	NP_001276718.1:p.Asn586=
NM_001289790.1:c.1557C>T	NP_001276719.1:p.Asn519=
XM_005258764.1:c.1641C>T	XP_005258821.1:p.Asn547=
XM_006723148.1:c.1641C>T	XP_006723211.1:p.Asn547=
XM_011526754.1:c.1758C>T	XP_011525056.1:p.Asn586=
NM_000175.5:c.1641C>T MANE Select	NP_000166.2:p.Asn547=
NM_001289790.2:c.1557C>T	NP_001276719.1:p.Asn519=
NM_001329909.1:c.1641C>T	NP_001316838.1:p.Asn547=
NM_001329910.1:c.1641C>T	NP_001316839.1:p.Asn547=
NM_001329911.1:c.1614C>T	NP_001316840.1:p.Asn538=
XM_011526754.3:c.1758C>T	XP_011525056.1:p.Asn586=
NM_001289790.3:c.1557C>T	NP_001276719.1:p.Asn519=
NM_001329911.2:c.1614C>T	NP_001316840.1:p.Asn538=