Canonical Allele Identifier: CA2701851793
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2106431616

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877415_240877416del , CM000664.2:g.240877415_240877416del GRCh38
NC_000002.11:g.241816832_241816833del , CM000664.1:g.241816832_241816833del GRCh37
NC_000002.10:g.241465505_241465506del NCBI36
NG_008005.1:g.13671_13672del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.847-122_847-121del MANE Select ENSP00000302620.3:n.847-122_847-121del
ENST00000307503.3:c.847-122_847-121del ENSP00000302620.3:n.847-122_847-121del
ENST00000470255.1:n.503_504del
NM_000030.2:c.847-122_847-121del NP_000021.1:n.847-122_847-121del
NM_000030.3:c.847-122_847-121del MANE Select NP_000021.1:n.847-122_847-121del