Canonical Allele Identifier: CA2695139611
Gene: G6PD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154531468_154531471del , CM000685.2:g.154531468_154531471del GRCh38
NC_000023.10:g.153759683_153759686del , CM000685.1:g.153759683_153759686del GRCh37
NC_000023.9:g.153412877_153412880del NCBI36
NG_009015.2:g.21104_21107del

Transcript Alleles

HGVS Amino-acid Change
ENST00000393564.7:c.*531_*534del ENSP00000377194.2:n.*531_*534del
ENST00000439227.6:c.*531_*534del ENSP00000395599.2:n.*531_*534del
ENST00000696420.1:c.1457+719_1457+722del ENSP00000512615.1:n.1457+719_1457+722del
ENST00000696421.1:c.1457+719_1457+722del ENSP00000512616.1:n.1457+719_1457+722del
ENST00000696422.1:c.1942_1945del
ENST00000696423.1:c.1945_1948del
ENST00000696424.1:c.1931_1934del ENSP00000512619.1:n.1931_1934del
ENST00000696425.1:c.*992_*995del ENSP00000512620.1:n.*992_*995del
ENST00000696426.1:c.*1539_*1542del ENSP00000512621.1:n.*1539_*1542del
ENST00000696427.1:c.*1039_*1042del ENSP00000512622.1:n.*1039_*1042del
ENST00000696428.1:c.*1921_*1924del ENSP00000512623.1:n.*1921_*1924del
ENST00000696429.1:c.*531_*534del ENSP00000512624.1:n.*531_*534del
ENST00000696430.1:c.*531_*534del ENSP00000512625.1:n.*531_*534del
ENST00000393562.10:c.*531_*534del MANE Select ENSP00000377192.3:n.*531_*534del
ENST00000393562.6:c.*531_*534del ENSP00000377192.2:n.*531_*534del
ENST00000621232.4:c.*531_*534del ENSP00000483686.1:n.*531_*534del
NM_000402.4:c.*531_*534del NP_000393.4:n.*531_*534del
NM_001042351.2:c.*531_*534del NP_001035810.1:n.*531_*534del
XM_005274657.2:c.*531_*534del XP_005274714.1:n.*531_*534del
XM_005274658.2:c.*531_*534del XP_005274715.1:n.*531_*534del
NM_001360016.2:c.*531_*534del MANE Select NP_001346945.1:n.*531_*534del
NM_001042351.3:c.*531_*534del NP_001035810.1:n.*531_*534del