Canonical Allele Identifier: CA2843024411
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240874081dup , CM000664.2:g.240874081dup GRCh38
NC_000002.11:g.241813498dup , CM000664.1:g.241813498dup GRCh37
NC_000002.10:g.241462171dup NCBI36
NG_008005.1:g.10337dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.680+19dup MANE Select ENSP00000302620.3:n.680+19dup
ENST00000307503.3:c.680+19dup ENSP00000302620.3:n.680+19dup
ENST00000476698.1:n.333-1028dup
NM_000030.2:c.680+19dup NP_000021.1:n.680+19dup
NM_000030.3:c.680+19dup MANE Select NP_000021.1:n.680+19dup