Canonical Allele Identifier: CA2664012563
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878813_240878814del , CM000664.2:g.240878813_240878814del GRCh38
NC_000002.11:g.241818230_241818231del , CM000664.1:g.241818230_241818231del GRCh37
NC_000002.10:g.241466903_241466904del NCBI36
NG_008005.1:g.15069_15070del

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.1171_1172del MANE Select ENSP00000302620.3:p.Lys391AlafsTer21
ENST00000307503.3:c.1171_1172del ENSP00000302620.3:p.Lys391AlafsTer21
ENST00000470255.1:n.949_950del
NM_000030.2:c.1171_1172del NP_000021.1:p.Lys391AlafsTer21
NM_000030.3:c.1171_1172del MANE Select NP_000021.1:p.Lys391AlafsTer21