Canonical Allele Identifier: CA1226669577

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230710047_230710048delinsCA , CM000663.2:g.230710047_230710048delinsCA	GRCh38
NC_000001.10:g.230845793_230845794delinsCA , CM000663.1:g.230845793_230845794delinsCA	GRCh37
NC_000001.9:g.228912416_228912417delinsCA	NCBI36
NG_008836.1:g.9543_9544delinsTG
NG_008836.2:g.9543_9544delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.776_777delinsTG MANE Select	ENSP00000355627.5:p.Met259=
ENST00000679684.1:c.776_777delinsTG	ENSP00000505981.1:p.Met259=
ENST00000679738.1:c.776_777delinsTG	ENSP00000505063.1:p.Met259=
ENST00000679802.1:c.776_777delinsTG	ENSP00000505184.1:p.Met259=
ENST00000679854.1:n.1287_1288delinsTG
ENST00000679957.1:c.776_777delinsTG	ENSP00000506646.1:p.Met259=
ENST00000680041.1:c.776_777delinsTG	ENSP00000504866.1:p.Met259=
ENST00000680783.1:c.776_777delinsTG	ENSP00000506329.1:p.Met259=
ENST00000681269.1:c.776_777delinsTG	ENSP00000505985.1:p.Met259=
ENST00000681347.1:n.1287_1288delinsTG
ENST00000681514.1:c.776_777delinsTG	ENSP00000505963.1:p.Met259=
ENST00000681772.1:c.776_777delinsTG	ENSP00000505829.1:p.Met259=
ENST00000366667.4:c.803_804delinsTG	ENSP00000355627.4:p.Met268=
NM_000029.3:c.803_804delinsTG	NP_000020.1:p.Met268=
NM_000029.4:c.803_804delinsTG	NP_000020.1:p.Met268=
NM_001382817.3:c.776_777delinsTG	NP_001369746.2:p.Met259=
NM_001384479.1:c.776_777delinsTG MANE Select	NP_001371408.1:p.Met259=