Canonical Allele Identifier: CA2754892468
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877978del , CM000664.2:g.240877978del GRCh38
NC_000002.11:g.241817395del , CM000664.1:g.241817395del GRCh37
NC_000002.10:g.241466068del NCBI36
NG_008005.1:g.14234del

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.943-44del MANE Select ENSP00000302620.3:n.943-44del
ENST00000307503.3:c.943-44del ENSP00000302620.3:n.943-44del
ENST00000470255.1:n.721-44del
NM_000030.2:c.943-44del NP_000021.1:n.943-44del
NM_000030.3:c.943-44del MANE Select NP_000021.1:n.943-44del