Canonical Allele Identifier: CA1044064834
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869089_240869092del , CM000664.2:g.240869089_240869092del GRCh38
NC_000002.11:g.241808506_241808509del , CM000664.1:g.241808506_241808509del GRCh37
NC_000002.10:g.241457179_241457182del NCBI36
NG_008005.1:g.5345_5348del

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+59_165+62del MANE Select ENSP00000302620.3:n.165+59_165+62del
ENST00000307503.3:c.165+59_165+62del ENSP00000302620.3:n.165+59_165+62del
ENST00000472436.1:n.185+59_185+62del
NM_000030.2:c.165+59_165+62del NP_000021.1:n.165+59_165+62del
XR_924060.1:n.405+1141_405+1144del
NM_000030.3:c.165+59_165+62del MANE Select NP_000021.1:n.165+59_165+62del