Canonical Allele Identifier: CA2664005149
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869101_240869102insAGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAA , CM000664.2:g.240869101_240869102insAGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAA GRCh38
NC_000002.11:g.241808518_241808519insAGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAA , CM000664.1:g.241808518_241808519insAGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAA GRCh37
NC_000002.10:g.241457191_241457192insAGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAA NCBI36
NG_008005.1:g.5357_5358insAGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAA

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.166-69_166-68insAGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAA MANE Select ENSP00000302620.3:n.166-69_166-68insAGGGG...
ENST00000307503.3:c.166-69_166-68insAGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAA ENSP00000302620.3:n.166-69_166-68insAGGGG...
ENST00000472436.1:n.186-69_186-68insAGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAA
NM_000030.2:c.166-69_166-68insAGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAA NP_000021.1:n.166-69_166-68insAGGGGTCACTG...
XR_924060.1:n.405+1158_405+1159insTACAGGGGTGAGACCCAGGCCCCCCGAGTGAGGAAGCAGTGACCCCTTTCCCTCGTCCACGATCTGTGGGTGGG
NM_000030.3:c.166-69_166-68insAGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAA MANE Select NP_000021.1:n.166-69_166-68insAGGGGTCACTG...