Canonical Allele Identifier: CA2740130061
Gene: G6PD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154534468G= , CM000685.2:g.154534468G= GRCh38
NC_000023.10:g.153762683G= , CM000685.1:g.153762683G= GRCh37
NC_000023.9:g.153415877G= NCBI36
NG_009015.2:g.18105C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393564.7:c.514C= ENSP00000377194.2:p.Pro172=
ENST00000439227.6:c.517C= ENSP00000395599.2:p.Pro173=
ENST00000696420.1:c.514C= ENSP00000512615.1:p.Pro172=
ENST00000696421.1:c.514C= ENSP00000512616.1:p.Pro172=
ENST00000696422.1:c.377C=
ENST00000696423.1:c.380C=
ENST00000696424.1:c.394C= ENSP00000512619.1:p.Pro132=
ENST00000696425.1:c.514C= ENSP00000512620.1:p.Pro172=
ENST00000696426.1:c.514C= ENSP00000512621.1:p.Pro172=
ENST00000696427.1:c.514C= ENSP00000512622.1:p.Pro172=
ENST00000696428.1:c.*356C= ENSP00000512623.1:n.*356C=
ENST00000696429.1:c.514C= ENSP00000512624.1:p.Pro172=
ENST00000696430.1:c.514C= ENSP00000512625.1:p.Pro172=
ENST00000393562.10:c.514C= MANE Select ENSP00000377192.3:p.Pro172=
ENST00000369620.6:c.514C= ENSP00000358633.2:p.Pro172=
ENST00000393562.6:c.604C= ENSP00000377192.2:p.Pro202=
ENST00000393564.6:c.514C= ENSP00000377194.2:p.Pro172=
ENST00000433845.1:c.514C= ENSP00000394690.1:p.Pro172=
ENST00000439227.5:c.517C= ENSP00000395599.1:p.Pro173=
ENST00000440967.5:c.517C= ENSP00000400648.1:p.Pro173=
ENST00000621232.4:c.514C= ENSP00000483686.1:p.Pro172=
NM_000402.4:c.604C= NP_000393.4:p.Pro202=
NM_001042351.2:c.514C= NP_001035810.1:p.Pro172=
XM_005274657.2:c.607C= XP_005274714.1:p.Pro203=
XM_005274658.2:c.517C= XP_005274715.1:p.Pro173=
XM_011531132.1:c.607C= XP_011529434.1:p.Pro203=
NM_001360016.2:c.514C= MANE Select NP_001346945.1:p.Pro172=
NM_001042351.3:c.514C= NP_001035810.1:p.Pro172=