Canonical Allele Identifier: CA1363482233
Gene: AMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49422187C= , CM000665.2:g.49422187C= GRCh38
NC_000003.11:g.49459620C= , CM000665.1:g.49459620C= GRCh37
NC_000003.10:g.49434624C= NCBI36
NG_015986.1:g.5492G= , LRG_537:g.5492G=
NG_033046.1:g.12138G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000273588.9:c.175G= MANE Select ENSP00000273588.3:p.Val59=
ENST00000395338.7:c.175G= ENSP00000378747.2:p.Val59=
ENST00000399379.7:c.60+174G= ENSP00000399943.2:n.60+174G=
ENST00000427987.6:c.31G= ENSP00000403821.2:p.Val11=
ENST00000430521.2:c.91-138G= ENSP00000388068.2:n.91-138G=
ENST00000462048.2:c.-101-138G= ENSP00000490465.1:n.-101-138G=
ENST00000465925.6:n.194G=
ENST00000473163.2:n.277G=
ENST00000476127.6:n.52G=
ENST00000476226.6:n.174G=
ENST00000478594.6:n.180G=
ENST00000480957.6:n.193G=
ENST00000485108.6:n.305G=
ENST00000487589.6:n.88G=
ENST00000491800.3:n.286G=
ENST00000493046.6:n.272G=
ENST00000538581.6:c.31G= ENSP00000443200.2:p.Val11=
ENST00000635772.1:n.179G=
ENST00000635808.1:c.175G= ENSP00000489620.1:p.Val59=
ENST00000635889.1:n.184G=
ENST00000635936.1:n.167G=
ENST00000636023.1:c.175G= ENSP00000489969.1:p.Val59=
ENST00000636070.1:c.91-138G= ENSP00000490160.1:n.91-138G=
ENST00000636148.1:n.245G=
ENST00000636166.1:c.496-615G= ENSP00000490106.1:n.496-615G=
ENST00000636199.1:c.175G= ENSP00000490871.1:p.Val59=
ENST00000636204.1:n.1457G=
ENST00000636461.1:c.3287G=
ENST00000636522.1:c.90+174G= ENSP00000489758.1:n.90+174G=
ENST00000636587.1:n.407G=
ENST00000636597.1:c.175G= ENSP00000490251.1:p.Val59=
ENST00000636725.1:n.165G=
ENST00000636803.1:n.165G=
ENST00000636865.1:c.31G= ENSP00000490601.1:p.Val11=
ENST00000636871.1:n.118G=
ENST00000636978.1:n.179G=
ENST00000636991.1:n.198G=
ENST00000637088.1:n.3730G=
ENST00000637114.1:n.167G=
ENST00000637268.1:n.180G=
ENST00000637291.1:n.183G=
ENST00000637442.1:n.1670G=
ENST00000637457.1:n.202G=
ENST00000637682.1:c.175G= ENSP00000489856.1:p.Val59=
ENST00000637684.1:n.277G=
ENST00000637821.1:c.91-138G= ENSP00000490482.1:n.91-138G=
ENST00000637914.1:n.194G=
ENST00000637982.1:n.167G=
ENST00000637994.1:n.185G=
ENST00000638014.1:c.2956G=
ENST00000638063.1:c.175G= ENSP00000489760.1:p.Val59=
ENST00000638079.1:c.*691G= ENSP00000490120.1:n.*691G=
ENST00000638092.1:n.165G=
ENST00000638115.1:c.*1936G= ENSP00000490296.1:n.*1936G=
ENST00000273588.7:c.175G= ENSP00000273588.3:p.Val59=
ENST00000395338.6:c.175G= ENSP00000378747.2:p.Val59=
ENST00000399379.6:c.91-138G= ENSP00000399943.1:n.91-138G=
ENST00000427987.5:c.167G=
ENST00000430521.1:c.90+174G= ENSP00000388068.1:n.90+174G=
ENST00000458307.6:c.175G= ENSP00000415619.2:p.Val59=
ENST00000462048.1:n.248-138G=
ENST00000476226.5:n.240G=
ENST00000478594.5:n.169G=
ENST00000480957.5:n.183G=
ENST00000485108.5:n.169G=
ENST00000487589.5:n.277G=
ENST00000493046.5:n.92-138G=
ENST00000495436.5:n.265G=
ENST00000498571.1:n.173G=
ENST00000538581.5:c.90+174G= ENSP00000443200.1:n.90+174G=
NM_000481.3:c.175G= , LRG_537t1:c.175G= NP_000472.2:p.Val59=
NM_001164710.1:c.175G= NP_001158182.1:p.Val59=
NM_001164711.1:c.90+174G= NP_001158183.1:n.90+174G=
NM_001164712.1:c.175G= NP_001158184.1:p.Val59=
NR_028435.1:n.389G=
NM_000481.4:c.175G= MANE Select NP_000472.2:p.Val59=
NM_001164710.2:c.175G= NP_001158182.1:p.Val59=
NM_001164711.2:c.90+174G= NP_001158183.1:n.90+174G=
NM_001164712.2:c.175G= NP_001158184.1:p.Val59=
NR_028435.2:n.184G=