Canonical Allele Identifier: CA2664008744
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875054del , CM000664.2:g.240875054del GRCh38
NC_000002.11:g.241814471del , CM000664.1:g.241814471del GRCh37
NC_000002.10:g.241463144del NCBI36
NG_008005.1:g.11310del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.681-55del MANE Select ENSP00000302620.3:n.681-55del
ENST00000307503.3:c.681-55del ENSP00000302620.3:n.681-55del
ENST00000476698.1:n.333-55del
NM_000030.2:c.681-55del NP_000021.1:n.681-55del
NM_000030.3:c.681-55del MANE Select NP_000021.1:n.681-55del