Canonical Allele Identifier: CA2664006108
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869389_240869390insATCCAGGGCCAT , CM000664.2:g.240869389_240869390insATCCAGGGCCAT GRCh38
NC_000002.11:g.241808806_241808807insATCCAGGGCCAT , CM000664.1:g.241808806_241808807insATCCAGGGCCAT GRCh37
NC_000002.10:g.241457479_241457480insATCCAGGGCCAT NCBI36
NG_008005.1:g.5645_5646insATCCAGGGCCAT

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.358+27_358+28insATCCAGGGCCAT MANE Select ENSP00000302620.3:n.358+27_358+28insATCCA...
ENST00000307503.3:c.358+27_358+28insATCCAGGGCCAT ENSP00000302620.3:n.358+27_358+28insATCCA...
ENST00000472436.1:n.378+27_378+28insATCCAGGGCCAT
NM_000030.2:c.358+27_358+28insATCCAGGGCCAT NP_000021.1:n.358+27_358+28insATCCAGGGCCA...
XR_924060.1:n.405+843_405+844insATGGCCCTGGAT
NM_000030.3:c.358+27_358+28insATCCAGGGCCAT MANE Select NP_000021.1:n.358+27_358+28insATCCAGGGCCA...