Canonical Allele Identifier: CA1339335412
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877384_240877385delinsAG , CM000664.2:g.240877384_240877385delinsAG GRCh38
NC_000002.11:g.241816801_241816802delinsAG , CM000664.1:g.241816801_241816802delinsAG GRCh37
NC_000002.10:g.241465474_241465475delinsAG NCBI36
NG_008005.1:g.13640_13641delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.847-153_847-152delinsAG MANE Select ENSP00000302620.3:n.847-153_847-152delinsAG
ENST00000307503.3:c.847-153_847-152delinsAG ENSP00000302620.3:n.847-153_847-152delinsAG
ENST00000470255.1:n.472_473delinsAG
NM_000030.2:c.847-153_847-152delinsAG NP_000021.1:n.847-153_847-152delinsAG
NM_000030.3:c.847-153_847-152delinsAG MANE Select NP_000021.1:n.847-153_847-152delinsAG
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