Canonical Allele Identifier: CA647781043

Gene: AGXT

Linked Data

• COSMIC: COSN19526298

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240869077_240869078insCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC , CM000664.2:g.240869077_240869078insCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC	GRCh38
NC_000002.11:g.241808494_241808495insCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC , CM000664.1:g.241808494_241808495insCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC	GRCh37
NC_000002.10:g.241457167_241457168insCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC	NCBI36
NG_008005.1:g.5333_5334insCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC

Transcript Alleles

HGVS	Amino-acid change
ENST00000307503.4:c.165+47_165+48insCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC MANE Select	ENSP00000302620.3:n.165+47_165+48insCACCC...
ENST00000307503.3:c.165+47_165+48insCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC	ENSP00000302620.3:n.165+47_165+48insCACCC...
ENST00000472436.1:n.185+47_185+48insCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC
NM_000030.2:c.165+47_165+48insCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC	NP_000021.1:n.165+47_165+48insCACCCACAGAT...
XR_924060.1:n.405+1157_405+1158insTACAGGGGTGAGACCCAGGCCCCCCGAGTGAGGAAGCAGTGACCCCCTTCCCTCGTCCACGATCTGTGGGTGGG
NM_000030.3:c.165+47_165+48insCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACC MANE Select	NP_000021.1:n.165+47_165+48insCACCCACAGAT...