Canonical Allele Identifier: CA1226666971

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704081_230704091delinsCTCTTGCCCTG , CM000663.2:g.230704081_230704091delinsCTCTTGCCCTG	GRCh38
NC_000001.10:g.230839827_230839837delinsCTCTTGCCCTG , CM000663.1:g.230839827_230839837delinsCTCTTGCCCTG	GRCh37
NC_000001.9:g.228906450_228906460delinsCTCTTGCCCTG	NCBI36
NG_008836.1:g.15500_15510delinsCAGGGCAAGAG
NG_008836.2:g.15500_15510delinsCAGGGCAAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1242+102_1242+112delinsCAGGGCAAGAG MANE Select	ENSP00000355627.5:n.1242+102_1242+112delinsCAGGGCAAGAG
ENST00000679684.1:c.1242+102_1242+112delinsCAGGGCAAGAG	ENSP00000505981.1:n.1242+102_1242+112delinsCAGGGCAAGAG
ENST00000679738.1:c.1242+102_1242+112delinsCAGGGCAAGAG	ENSP00000505063.1:n.1242+102_1242+112delinsCAGGGCAAGAG
ENST00000679802.1:c.*701+102_*701+112delinsCAGGGCAAGAG	ENSP00000505184.1:n.*701+102_*701+112delinsCAGGGCAAGAG
ENST00000679854.1:n.5547+102_5547+112delinsCAGGGCAAGAG
ENST00000679957.1:c.1233+111_1233+121delinsCAGGGCAAGAG	ENSP00000506646.1:n.1233+111_1233+121delinsCAGGGCAAGAG
ENST00000680041.1:c.1242+102_1242+112delinsCAGGGCAAGAG	ENSP00000504866.1:n.1242+102_1242+112delinsCAGGGCAAGAG
ENST00000680783.1:c.829+5904_829+5914delinsCAGGGCAAGAG	ENSP00000506329.1:n.829+5904_829+5914delinsCAGGGCAAGAG
ENST00000681269.1:c.1242+102_1242+112delinsCAGGGCAAGAG	ENSP00000505985.1:n.1242+102_1242+112delinsCAGGGCAAGAG
ENST00000681347.1:n.3348+102_3348+112delinsCAGGGCAAGAG
ENST00000681514.1:c.1242+102_1242+112delinsCAGGGCAAGAG	ENSP00000505963.1:n.1242+102_1242+112delinsCAGGGCAAGAG
ENST00000681772.1:c.*736+102_*736+112delinsCAGGGCAAGAG	ENSP00000505829.1:n.*736+102_*736+112delinsCAGGGCAAGAG
ENST00000366667.4:c.1269+102_1269+112delinsCAGGGCAAGAG	ENSP00000355627.4:n.1269+102_1269+112delinsCAGGGCAAGAG
NM_000029.3:c.1269+102_1269+112delinsCAGGGCAAGAG	NP_000020.1:n.1269+102_1269+112delinsCAGGGCAAGAG
NM_000029.4:c.1269+102_1269+112delinsCAGGGCAAGAG	NP_000020.1:n.1269+102_1269+112delinsCAGGGCAAGAG
NM_001382817.3:c.1242+102_1242+112delinsCAGGGCAAGAG	NP_001369746.2:n.1242+102_1242+112delinsCAGGGCAAGAG
NM_001384479.1:c.1242+102_1242+112delinsCAGGGCAAGAG MANE Select	NP_001371408.1:n.1242+102_1242+112delinsCAGGGCAAGAG