Canonical Allele Identifier: CA2664012218
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878609del , CM000664.2:g.240878609del GRCh38
NC_000002.11:g.241818026del , CM000664.1:g.241818026del GRCh37
NC_000002.10:g.241466699del NCBI36
NG_008005.1:g.14865del

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.1072-105del MANE Select ENSP00000302620.3:n.1072-105del
ENST00000307503.3:c.1072-105del ENSP00000302620.3:n.1072-105del
ENST00000470255.1:n.850-105del
NM_000030.2:c.1072-105del NP_000021.1:n.1072-105del
NM_000030.3:c.1072-105del MANE Select NP_000021.1:n.1072-105del