Canonical Allele Identifier: CA1339330738
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868879A= , CM000664.2:g.240868879A= GRCh38
NC_000002.11:g.241808296A= , CM000664.1:g.241808296A= GRCh37
NC_000002.10:g.241456969A= NCBI36
NG_008005.1:g.5135A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.14A= MANE Select ENSP00000302620.3:p.Lys5=
ENST00000307503.3:c.14A= ENSP00000302620.3:p.Lys5=
ENST00000472436.1:n.34A=
NM_000030.2:c.14A= NP_000021.1:p.Lys5=
XR_924060.1:n.405+1354T=
NM_000030.3:c.14A= MANE Select NP_000021.1:p.Lys5=