Canonical Allele Identifier: CA2664008170
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240874128_240874129dup , CM000664.2:g.240874128_240874129dup GRCh38
NC_000002.11:g.241813545_241813546dup , CM000664.1:g.241813545_241813546dup GRCh37
NC_000002.10:g.241462218_241462219dup NCBI36
NG_008005.1:g.10384_10385dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.680+66_680+67dup MANE Select ENSP00000302620.3:n.680+66_680+67dup
ENST00000307503.3:c.680+66_680+67dup ENSP00000302620.3:n.680+66_680+67dup
ENST00000476698.1:n.333-981_333-980dup
NM_000030.2:c.680+66_680+67dup NP_000021.1:n.680+66_680+67dup
NM_000030.3:c.680+66_680+67dup MANE Select NP_000021.1:n.680+66_680+67dup