Canonical Allele Identifier: CA405251454

Gene: GPI

Linked Data

• MyVariant Identifiers: chr19:g.34869888G>A (hg19) ; chr19:g.34378983G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34378983G>A , CM000681.2:g.34378983G>A	GRCh38
NC_000019.9:g.34869888G>A , CM000681.1:g.34869888G>A	GRCh37
NC_000019.8:g.39561728G>A	NCBI36
NG_012838.2:g.19244G>A
NG_012838.3:g.24392G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.683G>A MANE Select	ENSP00000348877.3:p.Trp228Ter
ENST00000415930.8:c.800G>A	ENSP00000405573.3:p.Trp267Ter
ENST00000586425.2:c.571G>A
ENST00000588991.7:c.716G>A	ENSP00000465858.3:p.Trp239Ter
ENST00000589399.6:c.452G>A	ENSP00000468201.2:p.Trp151Ter
ENST00000643067.1:n.1193G>A
ENST00000647446.1:c.683G>A	ENSP00000495129.1:p.Trp228Ter
ENST00000356487.9:c.683G>A	ENSP00000348877.3:p.Trp228Ter
ENST00000415930.7:c.716G>A	ENSP00000405573.2:p.Trp239Ter
ENST00000586425.1:c.683G>A	ENSP00000467670.2:p.Trp228Ter
ENST00000588991.6:c.728G>A	ENSP00000465858.2:p.Trp243Ter
ENST00000590362.1:n.6G>A
NM_000175.3:c.683G>A	NP_000166.2:p.Trp228Ter
NM_001184722.1:c.716G>A	NP_001171651.1:p.Trp239Ter
NM_001289789.1:c.800G>A	NP_001276718.1:p.Trp267Ter
NM_001289790.1:c.599G>A	NP_001276719.1:p.Trp200Ter
XM_005258764.1:c.683G>A	XP_005258821.1:p.Trp228Ter
XM_006723148.1:c.683G>A	XP_006723211.1:p.Trp228Ter
XM_011526754.1:c.800G>A	XP_011525056.1:p.Trp267Ter
XM_011526755.1:c.800G>A	XP_011525057.1:p.Trp267Ter
NM_000175.5:c.683G>A MANE Select	NP_000166.2:p.Trp228Ter
NM_001289790.2:c.599G>A	NP_001276719.1:p.Trp200Ter
NM_001329909.1:c.683G>A	NP_001316838.1:p.Trp228Ter
NM_001329910.1:c.683G>A	NP_001316839.1:p.Trp228Ter
NM_001329911.1:c.683G>A	NP_001316840.1:p.Trp228Ter
XM_011526754.3:c.800G>A	XP_011525056.1:p.Trp267Ter
NM_001289790.3:c.599G>A	NP_001276719.1:p.Trp200Ter
NM_001329911.2:c.683G>A	NP_001316840.1:p.Trp228Ter