Canonical Allele Identifier: CA68180080
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs398122324

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875987_240875988delinsA , CM000664.2:g.240875987_240875988delinsA GRCh38
NC_000002.11:g.241815404_241815405delinsA , CM000664.1:g.241815404_241815405delinsA GRCh37
NC_000002.10:g.241464077_241464078delinsA NCBI36
NG_008005.1:g.12243_12244delinsA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.829_830delinsA MANE Select ENSP00000302620.3:p.Ala277ThrfsTer?
ENST00000307503.3:c.829_830delinsA ENSP00000302620.3:p.Ala277ThrfsTer?
ENST00000476698.1:n.481_482delinsA
NM_000030.2:c.829_830delinsA NP_000021.1:p.Ala277ThrfsTer?
NM_000030.3:c.829_830delinsA MANE Select NP_000021.1:p.Ala277ThrfsTer?