Canonical Allele Identifier: CA1339332111
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240871414G= , CM000664.2:g.240871414G= GRCh38
NC_000002.11:g.241810831G= , CM000664.1:g.241810831G= GRCh37
NC_000002.10:g.241459504G= NCBI36
NG_008005.1:g.7670G=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.489G= MANE Select ENSP00000302620.3:p.Leu163=
ENST00000307503.3:c.489G= ENSP00000302620.3:p.Leu163=
ENST00000472436.1:n.509G=
ENST00000476698.1:n.226G=
NM_000030.2:c.489G= NP_000021.1:p.Leu163=
NM_000030.3:c.489G= MANE Select NP_000021.1:p.Leu163=