Canonical Allele Identifier: CA2673511967

Gene: AGXT2

Linked Data

• gnomAD v4: 5-34998846-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998847_34998848del , CM000667.2:g.34998847_34998848del	GRCh38
NC_000005.9:g.34998952_34998953del , CM000667.1:g.34998952_34998953del	GRCh37
NC_000005.8:g.35034709_35034710del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231420.11:c.1438-22_1438-21del MANE Select	ENSP00000231420.6:n.1438-22_1438-21del
ENST00000231420.10:c.1438-22_1438-21del	ENSP00000231420.6:n.1438-22_1438-21del
ENST00000510428.1:c.1213-22_1213-21del	ENSP00000422799.1:n.1213-22_1213-21del
ENST00000512135.5:n.1108-22_1108-21del
ENST00000618015.4:c.1213-22_1213-21del	ENSP00000479154.1:n.1213-22_1213-21del
NM_001306173.1:c.1213-22_1213-21del	NP_001293102.1:n.1213-22_1213-21del
NM_031900.3:c.1438-22_1438-21del	NP_114106.1:n.1438-22_1438-21del
XM_005248337.2:c.1435-22_1435-21del	XP_005248394.1:n.1435-22_1435-21del
XM_005248338.2:c.1243-22_1243-21del	XP_005248395.1:n.1243-22_1243-21del
XM_011514077.1:c.1438-446_1438-445del	XP_011512379.1:n.1438-446_1438-445del
XM_005248337.3:c.1435-22_1435-21del	XP_005248394.1:n.1435-22_1435-21del
XM_005248338.3:c.1243-22_1243-21del	XP_005248395.1:n.1243-22_1243-21del
XM_017009748.2:c.1213-22_1213-21del	XP_016865237.1:n.1213-22_1213-21del
NM_031900.4:c.1438-22_1438-21del MANE Select	NP_114106.1:n.1438-22_1438-21del
NM_001306173.2:c.1213-22_1213-21del	NP_001293102.1:n.1213-22_1213-21del