Canonical Allele Identifier: CA1339330853
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2058977042

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869076_240869077insTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC , CM000664.2:g.240869076_240869077insTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC GRCh38
NC_000002.11:g.241808493_241808494insTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC , CM000664.1:g.241808493_241808494insTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC GRCh37
NC_000002.10:g.241457166_241457167insTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC NCBI36
NG_008005.1:g.5332_5333insTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+46_165+47insTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC MANE Select ENSP00000302620.3:n.165+46_165+47insTCACT...
ENST00000307503.3:c.165+46_165+47insTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC ENSP00000302620.3:n.165+46_165+47insTCACT...
ENST00000472436.1:n.185+46_185+47insTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC
NM_000030.2:c.165+46_165+47insTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC NP_000021.1:n.165+46_165+47insTCACTCGGGGG...
XR_924060.1:n.405+1158_405+1159insTACAGGGGTGAGACCCAGGCCCCCCGAGTGAGG
NM_000030.3:c.165+46_165+47insTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC MANE Select NP_000021.1:n.165+46_165+47insTCACTCGGGGG...