Canonical Allele Identifier: CA2577302786
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878696_240878697insTCC , CM000664.2:g.240878696_240878697insTCC GRCh38
NC_000002.11:g.241818113_241818114insTCC , CM000664.1:g.241818113_241818114insTCC GRCh37
NC_000002.10:g.241466786_241466787insTCC NCBI36
NG_008005.1:g.14952_14953insTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1072-18_1072-17insTCC MANE Select ENSP00000302620.3:n.1072-18_1072-17insTCC
ENST00000307503.3:c.1072-18_1072-17insTCC ENSP00000302620.3:n.1072-18_1072-17insTCC
ENST00000470255.1:n.850-18_850-17insTCC
NM_000030.2:c.1072-18_1072-17insTCC NP_000021.1:n.1072-18_1072-17insTCC
NM_000030.3:c.1072-18_1072-17insTCC MANE Select NP_000021.1:n.1072-18_1072-17insTCC