Canonical Allele Identifier: CA307634346

Gene: GPI

Linked Data

• dbSNP Id: rs929811872
• gnomAD v3: 19-34399590-T-C
• gnomAD v4: 19-34399590-T-C
• MyVariant Identifiers: chr19:g.34890495T>C (hg19) ; chr19:g.34399590T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399590T>C , CM000681.2:g.34399590T>C	GRCh38
NC_000019.9:g.34890495T>C , CM000681.1:g.34890495T>C	GRCh37
NC_000019.8:g.39582335T>C	NCBI36
NG_012838.2:g.39851T>C
NG_012838.3:g.44999T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1433T>C MANE Select	ENSP00000348877.3:p.Val478Ala
ENST00000415930.8:c.1550T>C	ENSP00000405573.3:p.Val517Ala
ENST00000586425.2:c.1158-146T>C
ENST00000588991.7:c.1466T>C	ENSP00000465858.3:p.Val489Ala
ENST00000643067.1:n.2478T>C
ENST00000647446.1:c.*484T>C	ENSP00000495129.1:n.*484T>C
ENST00000356487.9:c.1433T>C	ENSP00000348877.3:p.Val478Ala
ENST00000415930.7:c.1466T>C	ENSP00000405573.2:p.Val489Ala
ENST00000586077.1:n.2308T>C
ENST00000586392.1:n.1171T>C
ENST00000586425.1:c.1398+255T>C	ENSP00000467670.2:n.1398+255T>C
ENST00000588991.6:c.1478T>C	ENSP00000465858.2:p.Val493Ala
ENST00000592740.5:c.193+2933T>C
NM_000175.3:c.1433T>C	NP_000166.2:p.Val478Ala
NM_001184722.1:c.1466T>C	NP_001171651.1:p.Val489Ala
NM_001289789.1:c.1550T>C	NP_001276718.1:p.Val517Ala
NM_001289790.1:c.1349T>C	NP_001276719.1:p.Val450Ala
XM_005258764.1:c.1433T>C	XP_005258821.1:p.Val478Ala
XM_006723148.1:c.1433T>C	XP_006723211.1:p.Val478Ala
XM_011526754.1:c.1550T>C	XP_011525056.1:p.Val517Ala
NM_000175.5:c.1433T>C MANE Select	NP_000166.2:p.Val478Ala
NM_001289790.2:c.1349T>C	NP_001276719.1:p.Val450Ala
NM_001329909.1:c.1433T>C	NP_001316838.1:p.Val478Ala
NM_001329910.1:c.1433T>C	NP_001316839.1:p.Val478Ala
NM_001329911.1:c.1406T>C	NP_001316840.1:p.Val469Ala
XM_011526754.3:c.1550T>C	XP_011525056.1:p.Val517Ala
NM_001289790.3:c.1349T>C	NP_001276719.1:p.Val450Ala
NM_001329911.2:c.1406T>C	NP_001316840.1:p.Val469Ala