Canonical Allele Identifier: CA1339330820
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869032_240869035delinsTAGG , CM000664.2:g.240869032_240869035delinsTAGG GRCh38
NC_000002.11:g.241808449_241808452delinsTAGG , CM000664.1:g.241808449_241808452delinsTAGG GRCh37
NC_000002.10:g.241457122_241457125delinsTAGG NCBI36
NG_008005.1:g.5288_5291delinsTAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+2_165+5delinsTAGG MANE Select ENSP00000302620.3:n.165+2_165+5delinsTAGG...
ENST00000307503.3:c.165+2_165+5delinsTAGG ENSP00000302620.3:n.165+2_165+5delinsTAGG...
ENST00000472436.1:n.185+2_185+5delinsTAGG
NM_000030.2:c.165+2_165+5delinsTAGG NP_000021.1:n.165+2_165+5delinsTAGG
XR_924060.1:n.405+1198_405+1201delinsCCTA
NM_000030.3:c.165+2_165+5delinsTAGG MANE Select NP_000021.1:n.165+2_165+5delinsTAGG