Canonical Allele Identifier: CA506696039

Gene: GPI

Linked Data

• MyVariant Identifiers: chr19:g.34869880G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34378975G>C , CM000681.2:g.34378975G>C	GRCh38
NC_000019.9:g.34869880G>C , CM000681.1:g.34869880G>C	GRCh37
NC_000019.8:g.39561720G>C	NCBI36
NG_012838.2:g.19236G>C
NG_012838.3:g.24384G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000356487.11:c.675G>C MANE Select	ENSP00000348877.3:p.Ala225=
ENST00000415930.8:c.792G>C	ENSP00000405573.3:p.Ala264=
ENST00000586425.2:c.563G>C
ENST00000588991.7:c.708G>C	ENSP00000465858.3:p.Ala236=
ENST00000589399.6:c.444G>C	ENSP00000468201.2:p.Ala148=
ENST00000643067.1:n.1185G>C
ENST00000647446.1:c.675G>C	ENSP00000495129.1:p.Ala225=
ENST00000356487.9:c.675G>C	ENSP00000348877.3:p.Ala225=
ENST00000415930.7:c.708G>C	ENSP00000405573.2:p.Ala236=
ENST00000586425.1:c.675G>C	ENSP00000467670.2:p.Ala225=
ENST00000588991.6:c.720G>C	ENSP00000465858.2:p.Ala240=
NM_000175.3:c.675G>C	NP_000166.2:p.Ala225=
NM_001184722.1:c.708G>C	NP_001171651.1:p.Ala236=
NM_001289789.1:c.792G>C	NP_001276718.1:p.Ala264=
NM_001289790.1:c.591G>C	NP_001276719.1:p.Ala197=
XM_005258764.1:c.675G>C	XP_005258821.1:p.Ala225=
XM_006723148.1:c.675G>C	XP_006723211.1:p.Ala225=
XM_011526754.1:c.792G>C	XP_011525056.1:p.Ala264=
XM_011526755.1:c.792G>C	XP_011525057.1:p.Ala264=
NM_000175.5:c.675G>C MANE Select	NP_000166.2:p.Ala225=
NM_001289790.2:c.591G>C	NP_001276719.1:p.Ala197=
NM_001329909.1:c.675G>C	NP_001316838.1:p.Ala225=
NM_001329910.1:c.675G>C	NP_001316839.1:p.Ala225=
NM_001329911.1:c.675G>C	NP_001316840.1:p.Ala225=
XM_011526754.3:c.792G>C	XP_011525056.1:p.Ala264=
NM_001289790.3:c.591G>C	NP_001276719.1:p.Ala197=
NM_001329911.2:c.675G>C	NP_001316840.1:p.Ala225=