Canonical Allele Identifier: CA2664013854
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879166_240879167insAGC , CM000664.2:g.240879166_240879167insAGC GRCh38
NC_000002.11:g.241818583_241818584insAGC , CM000664.1:g.241818583_241818584insAGC GRCh37
NC_000002.10:g.241467256_241467257insAGC NCBI36
NG_008005.1:g.15422_15423insAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*345_*346insAGC MANE Select ENSP00000302620.3:n.*345_*346insAGC
ENST00000470255.1:n.1302_1303insAGC
NM_000030.3:c.*345_*346insAGC MANE Select NP_000021.1:n.*345_*346insAGC