Canonical Allele Identifier: CA2695139716

Gene: G6PD

Linked Data

• gnomAD v4: X-154531505-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154531505T>G , CM000685.2:g.154531505T>G	GRCh38
NC_000023.10:g.153759720T>G , CM000685.1:g.153759720T>G	GRCh37
NC_000023.9:g.153412914T>G	NCBI36
NG_009015.2:g.21068A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.*495A>C	ENSP00000377194.2:n.*495A>C
ENST00000439227.6:c.*495A>C	ENSP00000395599.2:n.*495A>C
ENST00000696420.1:c.1457+683A>C	ENSP00000512615.1:n.1457+683A>C
ENST00000696421.1:c.1457+683A>C	ENSP00000512616.1:n.1457+683A>C
ENST00000696422.1:c.1906A>C
ENST00000696423.1:c.1909A>C
ENST00000696424.1:c.1895A>C	ENSP00000512619.1:n.1895A>C
ENST00000696425.1:c.*956A>C	ENSP00000512620.1:n.*956A>C
ENST00000696426.1:c.*1503A>C	ENSP00000512621.1:n.*1503A>C
ENST00000696427.1:c.*1003A>C	ENSP00000512622.1:n.*1003A>C
ENST00000696428.1:c.*1885A>C	ENSP00000512623.1:n.*1885A>C
ENST00000696429.1:c.*495A>C	ENSP00000512624.1:n.*495A>C
ENST00000696430.1:c.*495A>C	ENSP00000512625.1:n.*495A>C
ENST00000393562.10:c.*495A>C MANE Select	ENSP00000377192.3:n.*495A>C
ENST00000393562.6:c.*495A>C	ENSP00000377192.2:n.*495A>C
ENST00000621232.4:c.*495A>C	ENSP00000483686.1:n.*495A>C
NM_000402.4:c.*495A>C	NP_000393.4:n.*495A>C
NM_001042351.2:c.*495A>C	NP_001035810.1:n.*495A>C
XM_005274657.2:c.*495A>C	XP_005274714.1:n.*495A>C
XM_005274658.2:c.*495A>C	XP_005274715.1:n.*495A>C
NM_001360016.2:c.*495A>C MANE Select	NP_001346945.1:n.*495A>C
NM_001042351.3:c.*495A>C	NP_001035810.1:n.*495A>C