Canonical Allele Identifier: CA2748101264
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230714163_230714166del , CM000663.2:g.230714163_230714166del GRCh38
NC_000001.10:g.230849909_230849912del , CM000663.1:g.230849909_230849912del GRCh37
NC_000001.9:g.228916532_228916535del NCBI36
NG_008836.1:g.5425_5428del
NG_008836.2:g.5425_5428del

Transcript Alleles

HGVS Amino-acid change
ENST00000679684.1:c.-111_-108del ENSP00000505981.1:n.-111_-108del
ENST00000679738.1:c.-111_-108del ENSP00000505063.1:n.-111_-108del
ENST00000679802.1:c.-111_-108del ENSP00000505184.1:n.-111_-108del
ENST00000679854.1:n.401_404del
ENST00000679957.1:c.-111_-108del ENSP00000506646.1:n.-111_-108del
ENST00000680783.1:c.-111_-108del ENSP00000506329.1:n.-111_-108del
ENST00000681269.1:c.-30-3313_-30-3310del ENSP00000505985.1:n.-30-3313_-30-3310del
ENST00000681347.1:n.401_404del
ENST00000681772.1:c.-111_-108del ENSP00000505829.1:n.-111_-108del
ENST00000366667.4:c.-84_-81del ENSP00000355627.4:n.-84_-81del
NM_000029.3:c.-84_-81del NP_000020.1:n.-84_-81del
NM_001382817.3:c.-30-3313_-30-3310del NP_001369746.2:n.-30-3313_-30-3310del