Canonical Allele Identifier: CA1339330976
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869285T= , CM000664.2:g.240869285T= GRCh38
NC_000002.11:g.241808702T= , CM000664.1:g.241808702T= GRCh37
NC_000002.10:g.241457375T= NCBI36
NG_008005.1:g.5541T=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.281T= MANE Select ENSP00000302620.3:p.Leu94=
ENST00000307503.3:c.281T= ENSP00000302620.3:p.Leu94=
ENST00000472436.1:n.301T=
NM_000030.2:c.281T= NP_000021.1:p.Leu94=
XR_924060.1:n.405+948A=
NM_000030.3:c.281T= MANE Select NP_000021.1:p.Leu94=