Canonical Allele Identifier: CA2695197709
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 2671867
ClinVar RCV Id: RCV003448966

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869282_240869283insCACACTT , CM000664.2:g.240869282_240869283insCACACTT GRCh38
NC_000002.11:g.241808699_241808700insCACACTT , CM000664.1:g.241808699_241808700insCACACTT GRCh37
NC_000002.10:g.241457372_241457373insCACACTT NCBI36
NG_008005.1:g.5538_5539insCACACTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.278_279insCACACTT MANE Select ENSP00000302620.3:p.Leu94ThrfsTer?
ENST00000307503.3:c.278_279insCACACTT ENSP00000302620.3:p.Leu94ThrfsTer?
ENST00000472436.1:n.298_299insCACACTT
NM_000030.2:c.278_279insCACACTT NP_000021.1:p.Leu94ThrfsTer?
XR_924060.1:n.405+951_405+952insAGTGTGA
NM_000030.3:c.278_279insCACACTT MANE Select NP_000021.1:p.Leu94ThrfsTer?