Canonical Allele Identifier: CA2581477201

Gene: AGXT2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998673C>G , CM000667.2:g.34998673C>G	GRCh38
NC_000005.9:g.34998778C>G , CM000667.1:g.34998778C>G	GRCh37
NC_000005.8:g.35034535C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000231420.11:c.*46G>C MANE Select	ENSP00000231420.6:n.*46G>C
ENST00000231420.10:c.*46G>C	ENSP00000231420.6:n.*46G>C
ENST00000510428.1:c.*45+1G>C	ENSP00000422799.1:n.*45+1G>C
ENST00000512135.5:n.1261G>C
ENST00000618015.4:c.*46G>C	ENSP00000479154.1:n.*46G>C
NM_001306173.1:c.*45+1G>C	NP_001293102.1:n.*45+1G>C
NM_031900.3:c.*46G>C	NP_114106.1:n.*46G>C
XM_005248337.2:c.*46G>C	XP_005248394.1:n.*46G>C
XM_005248338.2:c.*46G>C	XP_005248395.1:n.*46G>C
XM_011514077.1:c.1438-271G>C	XP_011512379.1:n.1438-271G>C
XM_005248337.3:c.*46G>C	XP_005248394.1:n.*46G>C
XM_005248338.3:c.*46G>C	XP_005248395.1:n.*46G>C
XM_017009748.2:c.*46G>C	XP_016865237.1:n.*46G>C
NM_031900.4:c.*46G>C MANE Select	NP_114106.1:n.*46G>C
NM_001306173.2:c.*45+1G>C	NP_001293102.1:n.*45+1G>C