Canonical Allele Identifier: CA1363479616
Gene: AMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49417965G= , CM000665.2:g.49417965G= GRCh38
NC_000003.11:g.49455398G= , CM000665.1:g.49455398G= GRCh37
NC_000003.10:g.49430402G= NCBI36
NG_015986.1:g.9714C= , LRG_537:g.9714C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000273588.9:c.886C= MANE Select ENSP00000273588.3:p.Arg296=
ENST00000395338.7:c.886C= ENSP00000378747.2:p.Arg296=
ENST00000399379.7:c.618C= ENSP00000399943.2:n.618C=
ENST00000427987.6:c.742C= ENSP00000403821.2:p.Arg248=
ENST00000465925.6:n.2888C=
ENST00000473163.2:n.3502C=
ENST00000476127.6:n.1115C=
ENST00000476226.6:n.1307C=
ENST00000478594.6:n.1313C=
ENST00000493046.6:n.2750-247C=
ENST00000538581.6:c.742C= ENSP00000443200.2:p.Arg248=
ENST00000635772.1:n.1724C=
ENST00000635798.1:n.392-247C=
ENST00000635808.1:c.805C= ENSP00000489620.1:p.Arg269=
ENST00000635889.1:n.1379C=
ENST00000635907.1:n.592-247C=
ENST00000635936.1:n.1154C=
ENST00000636023.1:c.*59C= ENSP00000489969.1:n.*59C=
ENST00000636070.1:c.*666C= ENSP00000490160.1:n.*666C=
ENST00000636148.1:n.2939C=
ENST00000636166.1:c.1123C= ENSP00000490106.1:p.Arg375=
ENST00000636188.1:c.65C=
ENST00000636199.1:c.448C= ENSP00000490871.1:p.Arg150=
ENST00000636204.1:n.2168C=
ENST00000636461.1:c.4420C=
ENST00000636522.1:c.718C= ENSP00000489758.1:p.Arg240=
ENST00000636587.1:n.972C=
ENST00000636594.1:n.408C=
ENST00000636597.1:c.551-247C= ENSP00000490251.1:n.551-247C=
ENST00000636725.1:n.1602C=
ENST00000636803.1:n.1228C=
ENST00000636865.1:c.730C= ENSP00000490601.1:p.Arg244=
ENST00000636871.1:n.1251C=
ENST00000636978.1:n.998C=
ENST00000636991.1:n.1331C=
ENST00000637059.1:c.338C= ENSP00000490153.1:n.338C=
ENST00000637088.1:n.5698C=
ENST00000637114.1:n.986C=
ENST00000637268.1:n.1787C=
ENST00000637291.1:n.1620C=
ENST00000637442.1:n.3107C=
ENST00000637455.1:c.697C= ENSP00000489628.1:p.Arg233=
ENST00000637457.1:n.1747C=
ENST00000637527.1:n.178C=
ENST00000637682.1:c.878-247C= ENSP00000489856.1:n.878-247C=
ENST00000637684.1:n.1096C=
ENST00000637821.1:c.*1196C= ENSP00000490482.1:n.*1196C=
ENST00000637914.1:n.2780C=
ENST00000637982.1:n.1300C=
ENST00000637994.1:n.1426C=
ENST00000638014.1:c.3667C=
ENST00000638063.1:c.805C= ENSP00000489760.1:p.Arg269=
ENST00000638079.1:c.*1398C= ENSP00000490120.1:n.*1398C=
ENST00000638092.1:n.1406C=
ENST00000638115.1:c.*2647C= ENSP00000490296.1:n.*2647C=
ENST00000273588.7:c.886C= ENSP00000273588.3:p.Arg296=
ENST00000395338.6:c.886C= ENSP00000378747.2:p.Arg296=
ENST00000399379.6:c.*666C= ENSP00000399943.1:n.*666C=
ENST00000427987.5:c.878C=
ENST00000430521.1:c.718C= ENSP00000388068.1:p.Arg240=
ENST00000458307.6:c.754C= ENSP00000415619.2:p.Arg252=
ENST00000465925.5:n.2184C=
ENST00000473163.1:n.255C=
ENST00000476127.5:n.645C=
ENST00000476226.5:n.951C=
ENST00000495436.5:n.655-247C=
ENST00000538581.5:c.718C= ENSP00000443200.1:p.Arg240=
NM_000481.3:c.886C= , LRG_537t1:c.886C= NP_000472.2:p.Arg296=
NM_001164710.1:c.754C= NP_001158182.1:p.Arg252=
NM_001164711.1:c.718C= NP_001158183.1:p.Arg240=
NM_001164712.1:c.886C= NP_001158184.1:p.Arg296=
NR_028435.1:n.1100C=
NM_000481.4:c.886C= MANE Select NP_000472.2:p.Arg296=
NM_001164710.2:c.754C= NP_001158182.1:p.Arg252=
NM_001164711.2:c.718C= NP_001158183.1:p.Arg240=
NM_001164712.2:c.886C= NP_001158184.1:p.Arg296=
NR_028435.2:n.895C=