Canonical Allele Identifier: CA405246743
Gene: GPI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.34399981C>G , CM000681.2:g.34399981C>G GRCh38
NC_000019.9:g.34890886C>G , CM000681.1:g.34890886C>G GRCh37
NC_000019.8:g.39582726C>G NCBI36
NG_012838.2:g.40242C>G
NG_012838.3:g.45390C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000356487.11:c.1622C>G MANE Select ENSP00000348877.3:p.Ser541Cys
ENST00000415930.8:c.1739C>G ENSP00000405573.3:p.Ser580Cys
ENST00000586425.2:c.1288C>G
ENST00000588991.7:c.1655C>G ENSP00000465858.3:p.Ser552Cys
ENST00000643067.1:n.2667C>G
ENST00000647446.1:c.*673C>G ENSP00000495129.1:n.*673C>G
ENST00000356487.9:c.1622C>G ENSP00000348877.3:p.Ser541Cys
ENST00000415930.7:c.1655C>G ENSP00000405573.2:p.Ser552Cys
ENST00000586077.1:n.2699C>G
ENST00000586392.1:n.1360C>G
ENST00000586425.1:c.*54C>G ENSP00000467670.2:n.*54C>G
ENST00000588991.6:c.1667C>G ENSP00000465858.2:p.Ser556Cys
ENST00000592740.5:c.193+3324C>G
NM_000175.3:c.1622C>G NP_000166.2:p.Ser541Cys
NM_001184722.1:c.1655C>G NP_001171651.1:p.Ser552Cys
NM_001289789.1:c.1739C>G NP_001276718.1:p.Ser580Cys
NM_001289790.1:c.1538C>G NP_001276719.1:p.Ser513Cys
XM_005258764.1:c.1622C>G XP_005258821.1:p.Ser541Cys
XM_006723148.1:c.1622C>G XP_006723211.1:p.Ser541Cys
XM_011526754.1:c.1739C>G XP_011525056.1:p.Ser580Cys
NM_000175.5:c.1622C>G MANE Select NP_000166.2:p.Ser541Cys
NM_001289790.2:c.1538C>G NP_001276719.1:p.Ser513Cys
NM_001329909.1:c.1622C>G NP_001316838.1:p.Ser541Cys
NM_001329910.1:c.1622C>G NP_001316839.1:p.Ser541Cys
NM_001329911.1:c.1595C>G NP_001316840.1:p.Ser532Cys
XM_011526754.3:c.1739C>G XP_011525056.1:p.Ser580Cys
NM_001289790.3:c.1538C>G NP_001276719.1:p.Ser513Cys
NM_001329911.2:c.1595C>G NP_001316840.1:p.Ser532Cys