Canonical Allele Identifier: CA1339330945
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869224C= , CM000664.2:g.240869224C= GRCh38
NC_000002.11:g.241808641C= , CM000664.1:g.241808641C= GRCh37
NC_000002.10:g.241457314C= NCBI36
NG_008005.1:g.5480C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.220C= MANE Select ENSP00000302620.3:p.Leu74=
ENST00000307503.3:c.220C= ENSP00000302620.3:p.Leu74=
ENST00000472436.1:n.240C=
NM_000030.2:c.220C= NP_000021.1:p.Leu74=
XR_924060.1:n.405+1009G=
NM_000030.3:c.220C= MANE Select NP_000021.1:p.Leu74=