Canonical Allele Identifier: CA1339330764
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868919C= , CM000664.2:g.240868919C= GRCh38
NC_000002.11:g.241808336C= , CM000664.1:g.241808336C= GRCh37
NC_000002.10:g.241457009C= NCBI36
NG_008005.1:g.5175C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.54C= MANE Select ENSP00000302620.3:p.Leu18=
ENST00000307503.3:c.54C= ENSP00000302620.3:p.Leu18=
ENST00000472436.1:n.74C=
NM_000030.2:c.54C= NP_000021.1:p.Leu18=
XR_924060.1:n.405+1314G=
NM_000030.3:c.54C= MANE Select NP_000021.1:p.Leu18=