Canonical Allele Identifier: CA405246802

Gene: GPI

Linked Data

• MyVariant Identifiers: chr19:g.34890913A>C (hg19) ; chr19:g.34400008A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34400008A>C , CM000681.2:g.34400008A>C	GRCh38
NC_000019.9:g.34890913A>C , CM000681.1:g.34890913A>C	GRCh37
NC_000019.8:g.39582753A>C	NCBI36
NG_012838.2:g.40269A>C
NG_012838.3:g.45417A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1649A>C MANE Select	ENSP00000348877.3:p.Lys550Thr
ENST00000415930.8:c.1766A>C	ENSP00000405573.3:p.Lys589Thr
ENST00000586425.2:c.1315A>C
ENST00000588991.7:c.1682A>C	ENSP00000465858.3:p.Lys561Thr
ENST00000643067.1:n.2694A>C
ENST00000647446.1:c.*700A>C	ENSP00000495129.1:n.*700A>C
ENST00000356487.9:c.1649A>C	ENSP00000348877.3:p.Lys550Thr
ENST00000415930.7:c.1682A>C	ENSP00000405573.2:p.Lys561Thr
ENST00000586077.1:n.2726A>C
ENST00000586392.1:n.1387A>C
ENST00000586425.1:c.*81A>C	ENSP00000467670.2:n.*81A>C
ENST00000588991.6:c.1694A>C	ENSP00000465858.2:p.Lys565Thr
ENST00000592740.5:c.193+3351A>C
NM_000175.3:c.1649A>C	NP_000166.2:p.Lys550Thr
NM_001184722.1:c.1682A>C	NP_001171651.1:p.Lys561Thr
NM_001289789.1:c.1766A>C	NP_001276718.1:p.Lys589Thr
NM_001289790.1:c.1565A>C	NP_001276719.1:p.Lys522Thr
XM_005258764.1:c.1649A>C	XP_005258821.1:p.Lys550Thr
XM_006723148.1:c.1649A>C	XP_006723211.1:p.Lys550Thr
XM_011526754.1:c.1766A>C	XP_011525056.1:p.Lys589Thr
NM_000175.5:c.1649A>C MANE Select	NP_000166.2:p.Lys550Thr
NM_001289790.2:c.1565A>C	NP_001276719.1:p.Lys522Thr
NM_001329909.1:c.1649A>C	NP_001316838.1:p.Lys550Thr
NM_001329910.1:c.1649A>C	NP_001316839.1:p.Lys550Thr
NM_001329911.1:c.1622A>C	NP_001316840.1:p.Lys541Thr
XM_011526754.3:c.1766A>C	XP_011525056.1:p.Lys589Thr
NM_001289790.3:c.1565A>C	NP_001276719.1:p.Lys522Thr
NM_001329911.2:c.1622A>C	NP_001316840.1:p.Lys541Thr