Canonical Allele Identifier: CA1363482209
Gene: AMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49422168T= , CM000665.2:g.49422168T= GRCh38
NC_000003.11:g.49459601T= , CM000665.1:g.49459601T= GRCh37
NC_000003.10:g.49434605T= NCBI36
NG_015986.1:g.5511A= , LRG_537:g.5511A=
NG_033046.1:g.12157A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000273588.9:c.194A= MANE Select ENSP00000273588.3:p.His65=
ENST00000395338.7:c.194A= ENSP00000378747.2:p.His65=
ENST00000399379.7:c.60+193A= ENSP00000399943.2:n.60+193A=
ENST00000427987.6:c.50A= ENSP00000403821.2:p.His17=
ENST00000430521.2:c.91-119A= ENSP00000388068.2:n.91-119A=
ENST00000462048.2:c.-101-119A= ENSP00000490465.1:n.-101-119A=
ENST00000465925.6:n.213A=
ENST00000473163.2:n.296A=
ENST00000476127.6:n.71A=
ENST00000476226.6:n.193A=
ENST00000478594.6:n.199A=
ENST00000480957.6:n.212A=
ENST00000485108.6:n.324A=
ENST00000487589.6:n.107A=
ENST00000491800.3:n.305A=
ENST00000493046.6:n.291A=
ENST00000538581.6:c.50A= ENSP00000443200.2:p.His17=
ENST00000635772.1:n.198A=
ENST00000635808.1:c.194A= ENSP00000489620.1:p.His65=
ENST00000635889.1:n.203A=
ENST00000635936.1:n.186A=
ENST00000636023.1:c.194A= ENSP00000489969.1:p.His65=
ENST00000636070.1:c.91-119A= ENSP00000490160.1:n.91-119A=
ENST00000636148.1:n.264A=
ENST00000636166.1:c.496-596A= ENSP00000490106.1:n.496-596A=
ENST00000636199.1:c.194A= ENSP00000490871.1:p.His65=
ENST00000636204.1:n.1476A=
ENST00000636461.1:c.3306A=
ENST00000636522.1:c.90+193A= ENSP00000489758.1:n.90+193A=
ENST00000636587.1:n.426A=
ENST00000636597.1:c.194A= ENSP00000490251.1:p.His65=
ENST00000636725.1:n.184A=
ENST00000636803.1:n.184A=
ENST00000636865.1:c.50A= ENSP00000490601.1:p.His17=
ENST00000636871.1:n.137A=
ENST00000636978.1:n.198A=
ENST00000636991.1:n.217A=
ENST00000637059.1:c.5A= ENSP00000490153.1:p.His2=
ENST00000637088.1:n.3749A=
ENST00000637114.1:n.186A=
ENST00000637268.1:n.199A=
ENST00000637291.1:n.202A=
ENST00000637442.1:n.1689A=
ENST00000637455.1:c.5A= ENSP00000489628.1:p.His2=
ENST00000637457.1:n.221A=
ENST00000637682.1:c.194A= ENSP00000489856.1:p.His65=
ENST00000637684.1:n.296A=
ENST00000637821.1:c.91-119A= ENSP00000490482.1:n.91-119A=
ENST00000637914.1:n.213A=
ENST00000637982.1:n.186A=
ENST00000637994.1:n.204A=
ENST00000638014.1:c.2975A=
ENST00000638063.1:c.194A= ENSP00000489760.1:p.His65=
ENST00000638079.1:c.*710A= ENSP00000490120.1:n.*710A=
ENST00000638092.1:n.184A=
ENST00000638115.1:c.*1955A= ENSP00000490296.1:n.*1955A=
ENST00000273588.7:c.194A= ENSP00000273588.3:p.His65=
ENST00000395338.6:c.194A= ENSP00000378747.2:p.His65=
ENST00000399379.6:c.91-119A= ENSP00000399943.1:n.91-119A=
ENST00000427987.5:c.186A=
ENST00000430521.1:c.90+193A= ENSP00000388068.1:n.90+193A=
ENST00000458307.6:c.194A= ENSP00000415619.2:p.His65=
ENST00000462048.1:n.248-119A=
ENST00000476226.5:n.259A=
ENST00000478594.5:n.188A=
ENST00000480957.5:n.202A=
ENST00000485108.5:n.188A=
ENST00000487589.5:n.296A=
ENST00000493046.5:n.92-119A=
ENST00000495436.5:n.284A=
ENST00000498571.1:n.192A=
ENST00000538581.5:c.90+193A= ENSP00000443200.1:n.90+193A=
NM_000481.3:c.194A= , LRG_537t1:c.194A= NP_000472.2:p.His65=
NM_001164710.1:c.194A= NP_001158182.1:p.His65=
NM_001164711.1:c.90+193A= NP_001158183.1:n.90+193A=
NM_001164712.1:c.194A= NP_001158184.1:p.His65=
NR_028435.1:n.408A=
NM_000481.4:c.194A= MANE Select NP_000472.2:p.His65=
NM_001164710.2:c.194A= NP_001158182.1:p.His65=
NM_001164711.2:c.90+193A= NP_001158183.1:n.90+193A=
NM_001164712.2:c.194A= NP_001158184.1:p.His65=
NR_028435.2:n.203A=