Canonical Allele Identifier: CA2701851832
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2106431621

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877423_240877424del , CM000664.2:g.240877423_240877424del GRCh38
NC_000002.11:g.241816840_241816841del , CM000664.1:g.241816840_241816841del GRCh37
NC_000002.10:g.241465513_241465514del NCBI36
NG_008005.1:g.13679_13680del

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.847-114_847-113del MANE Select ENSP00000302620.3:n.847-114_847-113del
ENST00000307503.3:c.847-114_847-113del ENSP00000302620.3:n.847-114_847-113del
ENST00000470255.1:n.511_512del
NM_000030.2:c.847-114_847-113del NP_000021.1:n.847-114_847-113del
NM_000030.3:c.847-114_847-113del MANE Select NP_000021.1:n.847-114_847-113del