Canonical Allele Identifier: CA766960547
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1195944996

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869099del , CM000664.2:g.240869099del GRCh38
NC_000002.11:g.241808516del , CM000664.1:g.241808516del GRCh37
NC_000002.10:g.241457189del NCBI36
NG_008005.1:g.5355del

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+69del MANE Select ENSP00000302620.3:n.165+69del
ENST00000307503.3:c.165+69del ENSP00000302620.3:n.165+69del
ENST00000472436.1:n.185+69del
NM_000030.2:c.165+69del NP_000021.1:n.165+69del
XR_924060.1:n.405+1136del
NM_000030.3:c.165+69del MANE Select NP_000021.1:n.165+69del