Canonical Allele Identifier: CA351312784
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868905C>A , CM000664.2:g.240868905C>A GRCh38
NC_000002.11:g.241808322C>A , CM000664.1:g.241808322C>A GRCh37
NC_000002.10:g.241456995C>A NCBI36
NG_008005.1:g.5161C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.40C>A MANE Select ENSP00000302620.3:p.Leu14Met
ENST00000307503.3:c.40C>A ENSP00000302620.3:p.Leu14Met
ENST00000472436.1:n.60C>A
NM_000030.2:c.40C>A NP_000021.1:p.Leu14Met
XR_924060.1:n.405+1328G>T
NM_000030.3:c.40C>A MANE Select NP_000021.1:p.Leu14Met