Canonical Allele Identifier: CA405246735

Gene: GPI

Linked Data

• gnomAD v4: 19-34399978-C-T
• MyVariant Identifiers: chr19:g.34890883C>T (hg19) ; chr19:g.34399978C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399978C>T , CM000681.2:g.34399978C>T	GRCh38
NC_000019.9:g.34890883C>T , CM000681.1:g.34890883C>T	GRCh37
NC_000019.8:g.39582723C>T	NCBI36
NG_012838.2:g.40239C>T
NG_012838.3:g.45387C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1619C>T MANE Select	ENSP00000348877.3:p.Ala540Val
ENST00000415930.8:c.1736C>T	ENSP00000405573.3:p.Ala579Val
ENST00000586425.2:c.1285C>T
ENST00000588991.7:c.1652C>T	ENSP00000465858.3:p.Ala551Val
ENST00000643067.1:n.2664C>T
ENST00000647446.1:c.*670C>T	ENSP00000495129.1:n.*670C>T
ENST00000356487.9:c.1619C>T	ENSP00000348877.3:p.Ala540Val
ENST00000415930.7:c.1652C>T	ENSP00000405573.2:p.Ala551Val
ENST00000586077.1:n.2696C>T
ENST00000586392.1:n.1357C>T
ENST00000586425.1:c.*51C>T	ENSP00000467670.2:n.*51C>T
ENST00000588991.6:c.1664C>T	ENSP00000465858.2:p.Ala555Val
ENST00000592740.5:c.193+3321C>T
NM_000175.3:c.1619C>T	NP_000166.2:p.Ala540Val
NM_001184722.1:c.1652C>T	NP_001171651.1:p.Ala551Val
NM_001289789.1:c.1736C>T	NP_001276718.1:p.Ala579Val
NM_001289790.1:c.1535C>T	NP_001276719.1:p.Ala512Val
XM_005258764.1:c.1619C>T	XP_005258821.1:p.Ala540Val
XM_006723148.1:c.1619C>T	XP_006723211.1:p.Ala540Val
XM_011526754.1:c.1736C>T	XP_011525056.1:p.Ala579Val
NM_000175.5:c.1619C>T MANE Select	NP_000166.2:p.Ala540Val
NM_001289790.2:c.1535C>T	NP_001276719.1:p.Ala512Val
NM_001329909.1:c.1619C>T	NP_001316838.1:p.Ala540Val
NM_001329910.1:c.1619C>T	NP_001316839.1:p.Ala540Val
NM_001329911.1:c.1592C>T	NP_001316840.1:p.Ala531Val
XM_011526754.3:c.1736C>T	XP_011525056.1:p.Ala579Val
NM_001289790.3:c.1535C>T	NP_001276719.1:p.Ala512Val
NM_001329911.2:c.1592C>T	NP_001316840.1:p.Ala531Val