Canonical Allele Identifier: CA2765861776

Gene: AGXT2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998911_34998912insCACACCCAACAC , CM000667.2:g.34998911_34998912insCACACCCAACAC	GRCh38
NC_000005.9:g.34999016_34999017insCACACCCAACAC , CM000667.1:g.34999016_34999017insCACACCCAACAC	GRCh37
NC_000005.8:g.35034773_35034774insCACACCCAACAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231420.11:c.1438-86_1438-85insGTGTTGGGTGTG MANE Select	ENSP00000231420.6:n.1438-86_1438-85insGTGTTGGGTGTG
ENST00000231420.10:c.1438-86_1438-85insGTGTTGGGTGTG	ENSP00000231420.6:n.1438-86_1438-85insGTGTTGGGTGTG
ENST00000510428.1:c.1213-86_1213-85insGTGTTGGGTGTG	ENSP00000422799.1:n.1213-86_1213-85insGTGTTGGGTGTG
ENST00000512135.5:n.1108-86_1108-85insGTGTTGGGTGTG
ENST00000618015.4:c.1213-86_1213-85insGTGTTGGGTGTG	ENSP00000479154.1:n.1213-86_1213-85insGTGTTGGGTGTG
NM_001306173.1:c.1213-86_1213-85insGTGTTGGGTGTG	NP_001293102.1:n.1213-86_1213-85insGTGTTGGGTGTG
NM_031900.3:c.1438-86_1438-85insGTGTTGGGTGTG	NP_114106.1:n.1438-86_1438-85insGTGTTGGGTGTG
XM_005248337.2:c.1435-86_1435-85insGTGTTGGGTGTG	XP_005248394.1:n.1435-86_1435-85insGTGTTGGGTGTG
XM_005248338.2:c.1243-86_1243-85insGTGTTGGGTGTG	XP_005248395.1:n.1243-86_1243-85insGTGTTGGGTGTG
XM_011514077.1:c.1438-510_1438-509insGTGTTGGGTGTG	XP_011512379.1:n.1438-510_1438-509insGTGTTGGGTGTG
XM_005248337.3:c.1435-86_1435-85insGTGTTGGGTGTG	XP_005248394.1:n.1435-86_1435-85insGTGTTGGGTGTG
XM_005248338.3:c.1243-86_1243-85insGTGTTGGGTGTG	XP_005248395.1:n.1243-86_1243-85insGTGTTGGGTGTG
XM_017009748.2:c.1213-86_1213-85insGTGTTGGGTGTG	XP_016865237.1:n.1213-86_1213-85insGTGTTGGGTGTG
NM_031900.4:c.1438-86_1438-85insGTGTTGGGTGTG MANE Select	NP_114106.1:n.1438-86_1438-85insGTGTTGGGTGTG
NM_001306173.2:c.1213-86_1213-85insGTGTTGGGTGTG	NP_001293102.1:n.1213-86_1213-85insGTGTTGGGTGTG