Canonical Allele Identifier: CA2695140026
Gene: G6PD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154531578T>C , CM000685.2:g.154531578T>C GRCh38
NC_000023.10:g.153759793T>C , CM000685.1:g.153759793T>C GRCh37
NC_000023.9:g.153412987T>C NCBI36
NG_009015.2:g.20995A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000393564.7:c.*422A>G ENSP00000377194.2:n.*422A>G
ENST00000439227.6:c.*422A>G ENSP00000395599.2:n.*422A>G
ENST00000696420.1:c.1457+610A>G ENSP00000512615.1:n.1457+610A>G
ENST00000696421.1:c.1457+610A>G ENSP00000512616.1:n.1457+610A>G
ENST00000696422.1:c.1833A>G
ENST00000696423.1:c.1836A>G
ENST00000696424.1:c.1822A>G ENSP00000512619.1:n.1822A>G
ENST00000696425.1:c.*883A>G ENSP00000512620.1:n.*883A>G
ENST00000696426.1:c.*1430A>G ENSP00000512621.1:n.*1430A>G
ENST00000696427.1:c.*930A>G ENSP00000512622.1:n.*930A>G
ENST00000696428.1:c.*1812A>G ENSP00000512623.1:n.*1812A>G
ENST00000696429.1:c.*422A>G ENSP00000512624.1:n.*422A>G
ENST00000696430.1:c.*422A>G ENSP00000512625.1:n.*422A>G
ENST00000393562.10:c.*422A>G MANE Select ENSP00000377192.3:n.*422A>G
ENST00000393562.6:c.*422A>G ENSP00000377192.2:n.*422A>G
ENST00000621232.4:c.*422A>G ENSP00000483686.1:n.*422A>G
NM_000402.4:c.*422A>G NP_000393.4:n.*422A>G
NM_001042351.2:c.*422A>G NP_001035810.1:n.*422A>G
XM_005274657.2:c.*422A>G XP_005274714.1:n.*422A>G
XM_005274658.2:c.*422A>G XP_005274715.1:n.*422A>G
NM_001360016.2:c.*422A>G MANE Select NP_001346945.1:n.*422A>G
NM_001042351.3:c.*422A>G NP_001035810.1:n.*422A>G