Canonical Allele Identifier: CA1226667087
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230704351_230704353delinsGCA , CM000663.2:g.230704351_230704353delinsGCA GRCh38
NC_000001.10:g.230840097_230840099delinsGCA , CM000663.1:g.230840097_230840099delinsGCA GRCh37
NC_000001.9:g.228906720_228906722delinsGCA NCBI36
NG_008836.1:g.15238_15240delinsTGC
NG_008836.2:g.15238_15240delinsTGC

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.1098-16_1098-14delinsTGC MANE Select ENSP00000355627.5:n.1098-16_1098-14delins...
ENST00000679684.1:c.1098-16_1098-14delinsTGC ENSP00000505981.1:n.1098-16_1098-14delins...
ENST00000679738.1:c.1098-16_1098-14delinsTGC ENSP00000505063.1:n.1098-16_1098-14delins...
ENST00000679802.1:c.*557-16_*557-14delinsTGC ENSP00000505184.1:n.*557-16_*557-14delins...
ENST00000679854.1:n.5403-16_5403-14delinsTGC
ENST00000679957.1:c.1098-16_1098-14delinsTGC ENSP00000506646.1:n.1098-16_1098-14delins...
ENST00000680041.1:c.1098-16_1098-14delinsTGC ENSP00000504866.1:n.1098-16_1098-14delins...
ENST00000680783.1:c.829+5642_829+5644delinsTGC ENSP00000506329.1:n.829+5642_829+5644deli...
ENST00000681269.1:c.1098-16_1098-14delinsTGC ENSP00000505985.1:n.1098-16_1098-14delins...
ENST00000681347.1:n.3188_3190delinsTGC
ENST00000681514.1:c.1098-16_1098-14delinsTGC ENSP00000505963.1:n.1098-16_1098-14delins...
ENST00000681772.1:c.*592-16_*592-14delinsTGC ENSP00000505829.1:n.*592-16_*592-14delins...
ENST00000366667.4:c.1125-16_1125-14delinsTGC ENSP00000355627.4:n.1125-16_1125-14delins...
NM_000029.3:c.1125-16_1125-14delinsTGC NP_000020.1:n.1125-16_1125-14delinsTGC
NM_000029.4:c.1125-16_1125-14delinsTGC NP_000020.1:n.1125-16_1125-14delinsTGC
NM_001382817.3:c.1098-16_1098-14delinsTGC NP_001369746.2:n.1098-16_1098-14delinsTGC...
NM_001384479.1:c.1098-16_1098-14delinsTGC MANE Select NP_001371408.1:n.1098-16_1098-14delinsTGC...