Canonical Allele Identifier: CA1339330757
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868906T= , CM000664.2:g.240868906T= GRCh38
NC_000002.11:g.241808323T= , CM000664.1:g.241808323T= GRCh37
NC_000002.10:g.241456996T= NCBI36
NG_008005.1:g.5162T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.41T= MANE Select ENSP00000302620.3:p.Leu14=
ENST00000307503.3:c.41T= ENSP00000302620.3:p.Leu14=
ENST00000472436.1:n.61T=
NM_000030.2:c.41T= NP_000021.1:p.Leu14=
XR_924060.1:n.405+1327A=
NM_000030.3:c.41T= MANE Select NP_000021.1:p.Leu14=