Canonical Allele Identifier: CA2664005305

Gene: AGXT

Linked Data

• gnomAD v4: 2-240869094-CGAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240869096_240869098del , CM000664.2:g.240869096_240869098del	GRCh38
NC_000002.11:g.241808513_241808515del , CM000664.1:g.241808513_241808515del	GRCh37
NC_000002.10:g.241457186_241457188del	NCBI36
NG_008005.1:g.5352_5354del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.165+66_165+68del MANE Select	ENSP00000302620.3:n.165+66_165+68del
ENST00000307503.3:c.165+66_165+68del	ENSP00000302620.3:n.165+66_165+68del
ENST00000472436.1:n.185+66_185+68del
NM_000030.2:c.165+66_165+68del	NP_000021.1:n.165+66_165+68del
XR_924060.1:n.405+1136_405+1138del
NM_000030.3:c.165+66_165+68del MANE Select	NP_000021.1:n.165+66_165+68del