Canonical Allele Identifier: CA405251437

Gene: GPI

Linked Data

• MyVariant Identifiers: chr19:g.34869882A>T (hg19) ; chr19:g.34378977A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34378977A>T , CM000681.2:g.34378977A>T	GRCh38
NC_000019.9:g.34869882A>T , CM000681.1:g.34869882A>T	GRCh37
NC_000019.8:g.39561722A>T	NCBI36
NG_012838.2:g.19238A>T
NG_012838.3:g.24386A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.677A>T MANE Select	ENSP00000348877.3:p.Lys226Met
ENST00000415930.8:c.794A>T	ENSP00000405573.3:p.Lys265Met
ENST00000586425.2:c.565A>T
ENST00000588991.7:c.710A>T	ENSP00000465858.3:p.Lys237Met
ENST00000589399.6:c.446A>T	ENSP00000468201.2:p.Lys149Met
ENST00000643067.1:n.1187A>T
ENST00000647446.1:c.677A>T	ENSP00000495129.1:p.Lys226Met
ENST00000356487.9:c.677A>T	ENSP00000348877.3:p.Lys226Met
ENST00000415930.7:c.710A>T	ENSP00000405573.2:p.Lys237Met
ENST00000586425.1:c.677A>T	ENSP00000467670.2:p.Lys226Met
ENST00000588991.6:c.722A>T	ENSP00000465858.2:p.Lys241Met
NM_000175.3:c.677A>T	NP_000166.2:p.Lys226Met
NM_001184722.1:c.710A>T	NP_001171651.1:p.Lys237Met
NM_001289789.1:c.794A>T	NP_001276718.1:p.Lys265Met
NM_001289790.1:c.593A>T	NP_001276719.1:p.Lys198Met
XM_005258764.1:c.677A>T	XP_005258821.1:p.Lys226Met
XM_006723148.1:c.677A>T	XP_006723211.1:p.Lys226Met
XM_011526754.1:c.794A>T	XP_011525056.1:p.Lys265Met
XM_011526755.1:c.794A>T	XP_011525057.1:p.Lys265Met
NM_000175.5:c.677A>T MANE Select	NP_000166.2:p.Lys226Met
NM_001289790.2:c.593A>T	NP_001276719.1:p.Lys198Met
NM_001329909.1:c.677A>T	NP_001316838.1:p.Lys226Met
NM_001329910.1:c.677A>T	NP_001316839.1:p.Lys226Met
NM_001329911.1:c.677A>T	NP_001316840.1:p.Lys226Met
XM_011526754.3:c.794A>T	XP_011525056.1:p.Lys265Met
NM_001289790.3:c.593A>T	NP_001276719.1:p.Lys198Met
NM_001329911.2:c.677A>T	NP_001316840.1:p.Lys226Met