Canonical Allele Identifier: CA307634985

Gene: GPI

Linked Data

• dbSNP Id: rs113649392
• gnomAD v3: 19-34400076-C-G
• gnomAD v4: 19-34400076-C-G
• MyVariant Identifiers: chr19:g.34890981C>G (hg19) ; chr19:g.34400076C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34400076C>G , CM000681.2:g.34400076C>G	GRCh38
NC_000019.9:g.34890981C>G , CM000681.1:g.34890981C>G	GRCh37
NC_000019.8:g.39582821C>G	NCBI36
NG_012838.2:g.40337C>G
NG_012838.3:g.45485C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.*40C>G MANE Select	ENSP00000348877.3:n.*40C>G
ENST00000415930.8:c.*40C>G	ENSP00000405573.3:n.*40C>G
ENST00000586425.2:c.1383C>G
ENST00000588991.7:c.*40C>G	ENSP00000465858.3:n.*40C>G
ENST00000643067.1:n.2762C>G
ENST00000647446.1:c.*768C>G	ENSP00000495129.1:n.*768C>G
ENST00000356487.9:c.*40C>G	ENSP00000348877.3:n.*40C>G
ENST00000415930.7:c.*40C>G	ENSP00000405573.2:n.*40C>G
ENST00000586077.1:n.2794C>G
ENST00000586392.1:n.1455C>G
ENST00000586425.1:c.*149C>G	ENSP00000467670.2:n.*149C>G
ENST00000588991.6:c.1762C>G	ENSP00000465858.2:n.1762C>G
ENST00000592740.5:c.193+3419C>G
NM_000175.3:c.*40C>G	NP_000166.2:n.*40C>G
NM_001184722.1:c.*40C>G	NP_001171651.1:n.*40C>G
NM_001289789.1:c.*40C>G	NP_001276718.1:n.*40C>G
NM_001289790.1:c.*40C>G	NP_001276719.1:n.*40C>G
XM_005258764.1:c.*40C>G	XP_005258821.1:n.*40C>G
XM_006723148.1:c.*40C>G	XP_006723211.1:n.*40C>G
XM_011526754.1:c.*40C>G	XP_011525056.1:n.*40C>G
NM_000175.5:c.*40C>G MANE Select	NP_000166.2:n.*40C>G
NM_001289790.2:c.*40C>G	NP_001276719.1:n.*40C>G
NM_001329909.1:c.*40C>G	NP_001316838.1:n.*40C>G
NM_001329910.1:c.*40C>G	NP_001316839.1:n.*40C>G
NM_001329911.1:c.*40C>G	NP_001316840.1:n.*40C>G
XM_011526754.3:c.*40C>G	XP_011525056.1:n.*40C>G
NM_001289790.3:c.*40C>G	NP_001276719.1:n.*40C>G
NM_001329911.2:c.*40C>G	NP_001316840.1:n.*40C>G