Canonical Allele Identifier: CA2754891891

Gene: AGXT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240869103_240869104insCGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG , CM000664.2:g.240869103_240869104insCGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG	GRCh38
NC_000002.11:g.241808520_241808521insCGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG , CM000664.1:g.241808520_241808521insCGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG	GRCh37
NC_000002.10:g.241457193_241457194insCGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG	NCBI36
NG_008005.1:g.5359_5360insCGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000307503.4:c.166-67_166-66insCGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG MANE Select	ENSP00000302620.3:n.166-67_166-66insCGGTC...
ENST00000307503.3:c.166-67_166-66insCGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG	ENSP00000302620.3:n.166-67_166-66insCGGTC...
ENST00000472436.1:n.186-67_186-66insCGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG
NM_000030.2:c.166-67_166-66insCGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG	NP_000021.1:n.166-67_166-66insCGGTCACTGCT...
XR_924060.1:n.405+1158_405+1159insTACAGGGGTGAGACCCAGGCCCCCCGAGTGAGGAAGCAGTGACCGCCTTCCCTCGTCCACGATCTGTGGGTGGG
NM_000030.3:c.166-67_166-66insCGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG MANE Select	NP_000021.1:n.166-67_166-66insCGGTCACTGCT...