Canonical Allele Identifier: CA2664012817
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240878865-A-AG
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878865_240878866insG , CM000664.2:g.240878865_240878866insG GRCh38
NC_000002.11:g.241818282_241818283insG , CM000664.1:g.241818282_241818283insG GRCh37
NC_000002.10:g.241466955_241466956insG NCBI36
NG_008005.1:g.15121_15122insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*44_*45insG MANE Select ENSP00000302620.3:n.*44_*45insG
ENST00000307503.3:c.*44_*45insG ENSP00000302620.3:n.*44_*45insG
ENST00000470255.1:n.1001_1002insG
NM_000030.2:c.*44_*45insG NP_000021.1:n.*44_*45insG
NM_000030.3:c.*44_*45insG MANE Select NP_000021.1:n.*44_*45insG
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