Canonical Allele Identifier: CA2466722961
Gene: G6PD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154531588G= , CM000685.2:g.154531588G= GRCh38
NC_000023.10:g.153759803G= , CM000685.1:g.153759803G= GRCh37
NC_000023.9:g.153412997G= NCBI36
NG_009015.2:g.20985C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393564.7:c.*412C= ENSP00000377194.2:n.*412C=
ENST00000439227.6:c.*412C= ENSP00000395599.2:n.*412C=
ENST00000696420.1:c.1457+600C= ENSP00000512615.1:n.1457+600C=
ENST00000696421.1:c.1457+600C= ENSP00000512616.1:n.1457+600C=
ENST00000696422.1:c.1823C=
ENST00000696423.1:c.1826C=
ENST00000696424.1:c.1812C= ENSP00000512619.1:n.1812C=
ENST00000696425.1:c.*873C= ENSP00000512620.1:n.*873C=
ENST00000696426.1:c.*1420C= ENSP00000512621.1:n.*1420C=
ENST00000696427.1:c.*920C= ENSP00000512622.1:n.*920C=
ENST00000696428.1:c.*1802C= ENSP00000512623.1:n.*1802C=
ENST00000696429.1:c.*412C= ENSP00000512624.1:n.*412C=
ENST00000696430.1:c.*412C= ENSP00000512625.1:n.*412C=
ENST00000393562.10:c.*412C= MANE Select ENSP00000377192.3:n.*412C=
ENST00000393562.6:c.*412C= ENSP00000377192.2:n.*412C=
ENST00000621232.4:c.*412C= ENSP00000483686.1:n.*412C=
NM_000402.4:c.*412C= NP_000393.4:n.*412C=
NM_001042351.2:c.*412C= NP_001035810.1:n.*412C=
XM_005274657.2:c.*412C= XP_005274714.1:n.*412C=
XM_005274658.2:c.*412C= XP_005274715.1:n.*412C=
NM_001360016.2:c.*412C= MANE Select NP_001346945.1:n.*412C=
NM_001042351.3:c.*412C= NP_001035810.1:n.*412C=