Canonical Allele Identifier: CA1339334176
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875130G= , CM000664.2:g.240875130G= GRCh38
NC_000002.11:g.241814547G= , CM000664.1:g.241814547G= GRCh37
NC_000002.10:g.241463220G= NCBI36
NG_008005.1:g.11386G=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.702G= MANE Select ENSP00000302620.3:p.Lys234=
ENST00000307503.3:c.702G= ENSP00000302620.3:p.Lys234=
ENST00000476698.1:n.354G=
NM_000030.2:c.702G= NP_000021.1:p.Lys234=
NM_000030.3:c.702G= MANE Select NP_000021.1:p.Lys234=