Canonical Allele Identifier: CA405246625

Gene: GPI

Linked Data

• COSMIC: COSM2751827
• MyVariant Identifiers: chr19:g.34890830T>C (hg19) ; chr19:g.34399925T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399925T>C , CM000681.2:g.34399925T>C	GRCh38
NC_000019.9:g.34890830T>C , CM000681.1:g.34890830T>C	GRCh37
NC_000019.8:g.39582670T>C	NCBI36
NG_012838.2:g.40186T>C
NG_012838.3:g.45334T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1566T>C MANE Select	ENSP00000348877.3:p.Ala522=
ENST00000415930.8:c.1683T>C	ENSP00000405573.3:p.Ala561=
ENST00000586425.2:c.1232T>C
ENST00000588991.7:c.1599T>C	ENSP00000465858.3:p.Ala533=
ENST00000643067.1:n.2611T>C
ENST00000647446.1:c.*617T>C	ENSP00000495129.1:n.*617T>C
ENST00000356487.9:c.1566T>C	ENSP00000348877.3:p.Ala522=
ENST00000415930.7:c.1599T>C	ENSP00000405573.2:p.Ala533=
ENST00000586077.1:n.2643T>C
ENST00000586392.1:n.1304T>C
ENST00000586425.1:c.1423T>C	ENSP00000467670.2:p.Ter475Gln
ENST00000588991.6:c.1611T>C	ENSP00000465858.2:p.Ala537=
ENST00000592740.5:c.193+3268T>C
NM_000175.3:c.1566T>C	NP_000166.2:p.Ala522=
NM_001184722.1:c.1599T>C	NP_001171651.1:p.Ala533=
NM_001289789.1:c.1683T>C	NP_001276718.1:p.Ala561=
NM_001289790.1:c.1482T>C	NP_001276719.1:p.Ala494=
XM_005258764.1:c.1566T>C	XP_005258821.1:p.Ala522=
XM_006723148.1:c.1566T>C	XP_006723211.1:p.Ala522=
XM_011526754.1:c.1683T>C	XP_011525056.1:p.Ala561=
NM_000175.5:c.1566T>C MANE Select	NP_000166.2:p.Ala522=
NM_001289790.2:c.1482T>C	NP_001276719.1:p.Ala494=
NM_001329909.1:c.1566T>C	NP_001316838.1:p.Ala522=
NM_001329910.1:c.1566T>C	NP_001316839.1:p.Ala522=
NM_001329911.1:c.1539T>C	NP_001316840.1:p.Ala513=
XM_011526754.3:c.1683T>C	XP_011525056.1:p.Ala561=
NM_001289790.3:c.1482T>C	NP_001276719.1:p.Ala494=
NM_001329911.2:c.1539T>C	NP_001316840.1:p.Ala513=