Canonical Allele Identifier: CA405246476

Gene: GPI

Linked Data

• MyVariant Identifiers: chr19:g.34890663G>C (hg19) ; chr19:g.34399758G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399758G>C , CM000681.2:g.34399758G>C	GRCh38
NC_000019.9:g.34890663G>C , CM000681.1:g.34890663G>C	GRCh37
NC_000019.8:g.39582503G>C	NCBI36
NG_012838.2:g.40019G>C
NG_012838.3:g.45167G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1514G>C MANE Select	ENSP00000348877.3:p.Trp505Ser
ENST00000415930.8:c.1631G>C	ENSP00000405573.3:p.Trp544Ser
ENST00000586425.2:c.1180G>C
ENST00000588991.7:c.1547G>C	ENSP00000465858.3:p.Trp516Ser
ENST00000643067.1:n.2559G>C
ENST00000647446.1:c.*565G>C	ENSP00000495129.1:n.*565G>C
ENST00000356487.9:c.1514G>C	ENSP00000348877.3:p.Trp505Ser
ENST00000415930.7:c.1547G>C	ENSP00000405573.2:p.Trp516Ser
ENST00000586077.1:n.2476G>C
ENST00000586392.1:n.1252G>C
ENST00000586425.1:c.1399-143G>C	ENSP00000467670.2:n.1399-143G>C
ENST00000588991.6:c.1559G>C	ENSP00000465858.2:p.Trp520Ser
ENST00000592740.5:c.193+3101G>C
NM_000175.3:c.1514G>C	NP_000166.2:p.Trp505Ser
NM_001184722.1:c.1547G>C	NP_001171651.1:p.Trp516Ser
NM_001289789.1:c.1631G>C	NP_001276718.1:p.Trp544Ser
NM_001289790.1:c.1430G>C	NP_001276719.1:p.Trp477Ser
XM_005258764.1:c.1514G>C	XP_005258821.1:p.Trp505Ser
XM_006723148.1:c.1514G>C	XP_006723211.1:p.Trp505Ser
XM_011526754.1:c.1631G>C	XP_011525056.1:p.Trp544Ser
NM_000175.5:c.1514G>C MANE Select	NP_000166.2:p.Trp505Ser
NM_001289790.2:c.1430G>C	NP_001276719.1:p.Trp477Ser
NM_001329909.1:c.1514G>C	NP_001316838.1:p.Trp505Ser
NM_001329910.1:c.1514G>C	NP_001316839.1:p.Trp505Ser
NM_001329911.1:c.1487G>C	NP_001316840.1:p.Trp496Ser
XM_011526754.3:c.1631G>C	XP_011525056.1:p.Trp544Ser
NM_001289790.3:c.1430G>C	NP_001276719.1:p.Trp477Ser
NM_001329911.2:c.1487G>C	NP_001316840.1:p.Trp496Ser