Canonical Allele Identifier: CA2565957042

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154534442_154534443insTC , CM000685.2:g.154534442_154534443insTC	GRCh38
NC_000023.10:g.153762657_153762658insTC , CM000685.1:g.153762657_153762658insTC	GRCh37
NC_000023.9:g.153415851_153415852insTC	NCBI36
NG_009015.2:g.18130_18131insGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.539_540insGA	ENSP00000377194.2:p.Asp181MetfsTer?
ENST00000439227.6:c.542_543insGA	ENSP00000395599.2:p.Asp182MetfsTer?
ENST00000696420.1:c.539_540insGA	ENSP00000512615.1:p.Asp181MetfsTer?
ENST00000696421.1:c.539_540insGA	ENSP00000512616.1:p.Asp181MetfsTer?
ENST00000696422.1:c.402_403insGA
ENST00000696423.1:c.405_406insGA
ENST00000696424.1:c.419_420insGA	ENSP00000512619.1:p.Asp141MetfsTer?
ENST00000696425.1:c.539_540insGA	ENSP00000512620.1:p.Asp181MetfsTer?
ENST00000696426.1:c.539_540insGA	ENSP00000512621.1:p.Asp181MetfsTer?
ENST00000696427.1:c.539_540insGA	ENSP00000512622.1:p.Asp181MetfsTer?
ENST00000696428.1:c.*381_*382insGA	ENSP00000512623.1:n.*381_*382insGA
ENST00000696429.1:c.539_540insGA	ENSP00000512624.1:p.Asp181MetfsTer?
ENST00000696430.1:c.539_540insGA	ENSP00000512625.1:p.Asp181MetfsTer?
ENST00000393562.10:c.539_540insGA MANE Select	ENSP00000377192.3:p.Asp181MetfsTer?
ENST00000369620.6:c.539_540insGA	ENSP00000358633.2:p.Asp181MetfsTer?
ENST00000393562.6:c.629_630insGA	ENSP00000377192.2:p.Asp211MetfsTer?
ENST00000393564.6:c.539_540insGA	ENSP00000377194.2:p.Asp181MetfsTer?
ENST00000433845.1:c.539_540insGA	ENSP00000394690.1:p.Asp181MetfsTer?
ENST00000439227.5:c.542_543insGA	ENSP00000395599.1:p.Asp182MetfsTer?
ENST00000440967.5:c.542_543insGA	ENSP00000400648.1:p.Asp182MetfsTer?
ENST00000621232.4:c.539_540insGA	ENSP00000483686.1:p.Asp181MetfsTer?
NM_000402.4:c.629_630insGA	NP_000393.4:p.Asp211MetfsTer?
NM_001042351.2:c.539_540insGA	NP_001035810.1:p.Asp181MetfsTer?
XM_005274657.2:c.632_633insGA	XP_005274714.1:p.Asp212MetfsTer?
XM_005274658.2:c.542_543insGA	XP_005274715.1:p.Asp182MetfsTer?
XM_011531132.1:c.632_633insGA	XP_011529434.1:p.Asp212MetfsTer?
NM_001360016.2:c.539_540insGA MANE Select	NP_001346945.1:p.Asp181MetfsTer?
NM_001042351.3:c.539_540insGA	NP_001035810.1:p.Asp181MetfsTer?