Canonical Allele Identifier: CA1339330758
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868907G= , CM000664.2:g.240868907G= GRCh38
NC_000002.11:g.241808324G= , CM000664.1:g.241808324G= GRCh37
NC_000002.10:g.241456997G= NCBI36
NG_008005.1:g.5163G=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.42G= MANE Select ENSP00000302620.3:p.Leu14=
ENST00000307503.3:c.42G= ENSP00000302620.3:p.Leu14=
ENST00000472436.1:n.62G=
NM_000030.2:c.42G= NP_000021.1:p.Leu14=
XR_924060.1:n.405+1326C=
NM_000030.3:c.42G= MANE Select NP_000021.1:p.Leu14=