Canonical Allele Identifier: CA10654282
Gene: G6PD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154531643C= , CM000685.2:g.154531643C= GRCh38
NG_009015.2:g.20930G=

Transcript Alleles

HGVS Amino-acid change
ENST00000393564.7:c.*357G= ENSP00000377194.2:n.*357G=
ENST00000439227.6:c.*357G= ENSP00000395599.2:n.*357G=
ENST00000696420.1:c.1457+545G= ENSP00000512615.1:n.1457+545G=
ENST00000696421.1:c.1457+545G= ENSP00000512616.1:n.1457+545G=
ENST00000696422.1:c.1768G=
ENST00000696423.1:c.1771G=
ENST00000696424.1:c.1757G= ENSP00000512619.1:n.1757G=
ENST00000696425.1:c.*818G= ENSP00000512620.1:n.*818G=
ENST00000696426.1:c.*1365G= ENSP00000512621.1:n.*1365G=
ENST00000696427.1:c.*865G= ENSP00000512622.1:n.*865G=
ENST00000696428.1:c.*1747G= ENSP00000512623.1:n.*1747G=
ENST00000696429.1:c.*357G= ENSP00000512624.1:n.*357G=
ENST00000696430.1:c.*357G= ENSP00000512625.1:n.*357G=
ENST00000393562.10:c.*357G= MANE Select ENSP00000377192.3:n.*357G=
ENST00000393562.6:c.*357G= ENSP00000377192.2:n.*357G=
ENST00000621232.4:c.*357G= ENSP00000483686.1:n.*357G=
NM_000402.4:c.*357G= NP_000393.4:n.*357G=
NM_001042351.2:c.*357G= NP_001035810.1:n.*357G=
XM_005274657.2:c.*357G= XP_005274714.1:n.*357G=
XM_005274658.2:c.*357G= XP_005274715.1:n.*357G=
NM_001360016.2:c.*357G= MANE Select NP_001346945.1:n.*357G=
NM_001042351.3:c.*357G= NP_001035810.1:n.*357G=