Canonical Allele Identifier: CA1363482163
Gene: AMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49422153A= , CM000665.2:g.49422153A= GRCh38
NC_000003.11:g.49459586A= , CM000665.1:g.49459586A= GRCh37
NC_000003.10:g.49434590A= NCBI36
NG_015986.1:g.5526T= , LRG_537:g.5526T=
NG_033046.1:g.12172T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000273588.9:c.209T= MANE Select ENSP00000273588.3:p.Leu70=
ENST00000395338.7:c.209T= ENSP00000378747.2:p.Leu70=
ENST00000399379.7:c.60+208T= ENSP00000399943.2:n.60+208T=
ENST00000427987.6:c.65T= ENSP00000403821.2:p.Leu22=
ENST00000430521.2:c.91-104T= ENSP00000388068.2:n.91-104T=
ENST00000462048.2:c.-101-104T= ENSP00000490465.1:n.-101-104T=
ENST00000465925.6:n.228T=
ENST00000473163.2:n.311T=
ENST00000476127.6:n.86T=
ENST00000476226.6:n.208T=
ENST00000478594.6:n.214T=
ENST00000480957.6:n.227T=
ENST00000485108.6:n.339T=
ENST00000487589.6:n.122T=
ENST00000491800.3:n.320T=
ENST00000493046.6:n.306T=
ENST00000538581.6:c.65T= ENSP00000443200.2:p.Leu22=
ENST00000635772.1:n.213T=
ENST00000635808.1:c.209T= ENSP00000489620.1:p.Leu70=
ENST00000635889.1:n.218T=
ENST00000635936.1:n.201T=
ENST00000636023.1:c.209T= ENSP00000489969.1:p.Leu70=
ENST00000636070.1:c.91-104T= ENSP00000490160.1:n.91-104T=
ENST00000636148.1:n.279T=
ENST00000636166.1:c.496-581T= ENSP00000490106.1:n.496-581T=
ENST00000636199.1:c.209T= ENSP00000490871.1:p.Leu70=
ENST00000636204.1:n.1491T=
ENST00000636461.1:c.3321T=
ENST00000636522.1:c.90+208T= ENSP00000489758.1:n.90+208T=
ENST00000636587.1:n.441T=
ENST00000636597.1:c.209T= ENSP00000490251.1:p.Leu70=
ENST00000636725.1:n.199T=
ENST00000636803.1:n.199T=
ENST00000636865.1:c.65T= ENSP00000490601.1:p.Leu22=
ENST00000636871.1:n.152T=
ENST00000636978.1:n.213T=
ENST00000636991.1:n.232T=
ENST00000637059.1:c.20T= ENSP00000490153.1:p.Leu7=
ENST00000637088.1:n.3764T=
ENST00000637114.1:n.201T=
ENST00000637268.1:n.214T=
ENST00000637291.1:n.217T=
ENST00000637442.1:n.1704T=
ENST00000637455.1:c.20T= ENSP00000489628.1:p.Leu7=
ENST00000637457.1:n.236T=
ENST00000637682.1:c.209T= ENSP00000489856.1:p.Leu70=
ENST00000637684.1:n.311T=
ENST00000637821.1:c.91-104T= ENSP00000490482.1:n.91-104T=
ENST00000637914.1:n.228T=
ENST00000637982.1:n.201T=
ENST00000637994.1:n.219T=
ENST00000638014.1:c.2990T=
ENST00000638063.1:c.209T= ENSP00000489760.1:p.Leu70=
ENST00000638079.1:c.*725T= ENSP00000490120.1:n.*725T=
ENST00000638092.1:n.199T=
ENST00000638115.1:c.*1970T= ENSP00000490296.1:n.*1970T=
ENST00000273588.7:c.209T= ENSP00000273588.3:p.Leu70=
ENST00000395338.6:c.209T= ENSP00000378747.2:p.Leu70=
ENST00000399379.6:c.91-104T= ENSP00000399943.1:n.91-104T=
ENST00000427987.5:c.201T=
ENST00000430521.1:c.90+208T= ENSP00000388068.1:n.90+208T=
ENST00000458307.6:c.209T= ENSP00000415619.2:p.Leu70=
ENST00000462048.1:n.248-104T=
ENST00000476226.5:n.274T=
ENST00000478594.5:n.203T=
ENST00000480957.5:n.217T=
ENST00000485108.5:n.203T=
ENST00000487589.5:n.311T=
ENST00000493046.5:n.92-104T=
ENST00000495436.5:n.299T=
ENST00000498571.1:n.207T=
ENST00000538581.5:c.90+208T= ENSP00000443200.1:n.90+208T=
NM_000481.3:c.209T= , LRG_537t1:c.209T= NP_000472.2:p.Leu70=
NM_001164710.1:c.209T= NP_001158182.1:p.Leu70=
NM_001164711.1:c.90+208T= NP_001158183.1:n.90+208T=
NM_001164712.1:c.209T= NP_001158184.1:p.Leu70=
NR_028435.1:n.423T=
NM_000481.4:c.209T= MANE Select NP_000472.2:p.Leu70=
NM_001164710.2:c.209T= NP_001158182.1:p.Leu70=
NM_001164711.2:c.90+208T= NP_001158183.1:n.90+208T=
NM_001164712.2:c.209T= NP_001158184.1:p.Leu70=
NR_028435.2:n.218T=