Canonical Allele Identifier: CA2695197710
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 2664115
ClinVar RCV Id: RCV003445261

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869159_240869162delinsTGCATGCAAGAT , CM000664.2:g.240869159_240869162delinsTGCATGCAAGAT GRCh38
NC_000002.11:g.241808576_241808579delinsTGCATGCAAGAT , CM000664.1:g.241808576_241808579delinsTGCATGCAAGAT GRCh37
NC_000002.10:g.241457249_241457252delinsTGCATGCAAGAT NCBI36
NG_008005.1:g.5415_5418delinsTGCATGCAAGAT

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.166-11_166-8delinsTGCATGCAAGAT MANE Select ENSP00000302620.3:n.166-11_166-8delinsTGC...
ENST00000307503.3:c.166-11_166-8delinsTGCATGCAAGAT ENSP00000302620.3:n.166-11_166-8delinsTGC...
ENST00000472436.1:n.186-11_186-8delinsTGCATGCAAGAT
NM_000030.2:c.166-11_166-8delinsTGCATGCAAGAT NP_000021.1:n.166-11_166-8delinsTGCATGCAA...
XR_924060.1:n.405+1071_405+1074delinsATCTTGCATGCA
NM_000030.3:c.166-11_166-8delinsTGCATGCAAGAT MANE Select NP_000021.1:n.166-11_166-8delinsTGCATGCAA...