Canonical Allele Identifier: CA2664012798

Gene: AGXT

Linked Data

• gnomAD v4: 2-240878861-TCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240878863_240878864del , CM000664.2:g.240878863_240878864del	GRCh38
NC_000002.11:g.241818280_241818281del , CM000664.1:g.241818280_241818281del	GRCh37
NC_000002.10:g.241466953_241466954del	NCBI36
NG_008005.1:g.15119_15120del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.*42_*43del MANE Select	ENSP00000302620.3:n.*42_*43del
ENST00000307503.3:c.*42_*43del	ENSP00000302620.3:n.*42_*43del
ENST00000470255.1:n.999_1000del
NM_000030.2:c.*42_*43del	NP_000021.1:n.*42_*43del
NM_000030.3:c.*42_*43del MANE Select	NP_000021.1:n.*42_*43del