Canonical Allele Identifier: CA405246728

Gene: GPI

Linked Data

• MyVariant Identifiers: chr19:g.34890879G>T (hg19) ; chr19:g.34399974G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399974G>T , CM000681.2:g.34399974G>T	GRCh38
NC_000019.9:g.34890879G>T , CM000681.1:g.34890879G>T	GRCh37
NC_000019.8:g.39582719G>T	NCBI36
NG_012838.2:g.40235G>T
NG_012838.3:g.45383G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1615G>T MANE Select	ENSP00000348877.3:p.Asp539Tyr
ENST00000415930.8:c.1732G>T	ENSP00000405573.3:p.Asp578Tyr
ENST00000586425.2:c.1281G>T
ENST00000588991.7:c.1648G>T	ENSP00000465858.3:p.Asp550Tyr
ENST00000643067.1:n.2660G>T
ENST00000647446.1:c.*666G>T	ENSP00000495129.1:n.*666G>T
ENST00000356487.9:c.1615G>T	ENSP00000348877.3:p.Asp539Tyr
ENST00000415930.7:c.1648G>T	ENSP00000405573.2:p.Asp550Tyr
ENST00000586077.1:n.2692G>T
ENST00000586392.1:n.1353G>T
ENST00000586425.1:c.*47G>T	ENSP00000467670.2:n.*47G>T
ENST00000588991.6:c.1660G>T	ENSP00000465858.2:p.Asp554Tyr
ENST00000592740.5:c.193+3317G>T
NM_000175.3:c.1615G>T	NP_000166.2:p.Asp539Tyr
NM_001184722.1:c.1648G>T	NP_001171651.1:p.Asp550Tyr
NM_001289789.1:c.1732G>T	NP_001276718.1:p.Asp578Tyr
NM_001289790.1:c.1531G>T	NP_001276719.1:p.Asp511Tyr
XM_005258764.1:c.1615G>T	XP_005258821.1:p.Asp539Tyr
XM_006723148.1:c.1615G>T	XP_006723211.1:p.Asp539Tyr
XM_011526754.1:c.1732G>T	XP_011525056.1:p.Asp578Tyr
NM_000175.5:c.1615G>T MANE Select	NP_000166.2:p.Asp539Tyr
NM_001289790.2:c.1531G>T	NP_001276719.1:p.Asp511Tyr
NM_001329909.1:c.1615G>T	NP_001316838.1:p.Asp539Tyr
NM_001329910.1:c.1615G>T	NP_001316839.1:p.Asp539Tyr
NM_001329911.1:c.1588G>T	NP_001316840.1:p.Asp530Tyr
XM_011526754.3:c.1732G>T	XP_011525056.1:p.Asp578Tyr
NM_001289790.3:c.1531G>T	NP_001276719.1:p.Asp511Tyr
NM_001329911.2:c.1588G>T	NP_001316840.1:p.Asp530Tyr