Canonical Allele Identifier: CA2754891925
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869311_240869312insCAGGGGCT , CM000664.2:g.240869311_240869312insCAGGGGCT GRCh38
NC_000002.11:g.241808728_241808729insCAGGGGCT , CM000664.1:g.241808728_241808729insCAGGGGCT GRCh37
NC_000002.10:g.241457401_241457402insCAGGGGCT NCBI36
NG_008005.1:g.5567_5568insCAGGGGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.307_308insCAGGGGCT MANE Select ENSP00000302620.3:p.Gly103AlafsTer20
ENST00000307503.3:c.307_308insCAGGGGCT ENSP00000302620.3:p.Gly103AlafsTer20
ENST00000472436.1:n.327_328insCAGGGGCT
NM_000030.2:c.307_308insCAGGGGCT NP_000021.1:p.Gly103AlafsTer20
XR_924060.1:n.405+921_405+922insAGCCCCTG
NM_000030.3:c.307_308insCAGGGGCT MANE Select NP_000021.1:p.Gly103AlafsTer20