Canonical Allele Identifier: CA2664009144
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875302dup , CM000664.2:g.240875302dup GRCh38
NC_000002.11:g.241814719dup , CM000664.1:g.241814719dup GRCh37
NC_000002.10:g.241463392dup NCBI36
NG_008005.1:g.11558dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.776+98dup MANE Select ENSP00000302620.3:n.776+98dup
ENST00000307503.3:c.776+98dup ENSP00000302620.3:n.776+98dup
ENST00000476698.1:n.428+98dup
NM_000030.2:c.776+98dup NP_000021.1:n.776+98dup
NM_000030.3:c.776+98dup MANE Select NP_000021.1:n.776+98dup