Canonical Allele Identifier: CA352791049
Gene: AMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49422123T>C , CM000665.2:g.49422123T>C GRCh38
NC_000003.11:g.49459556T>C , CM000665.1:g.49459556T>C GRCh37
NC_000003.10:g.49434560T>C NCBI36
NG_015986.1:g.5556A>G , LRG_537:g.5556A>G
NG_033046.1:g.12202A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000273588.9:c.239A>G MANE Select ENSP00000273588.3:p.Asp80Gly
ENST00000395338.7:c.239A>G ENSP00000378747.2:p.Asp80Gly
ENST00000399379.7:c.60+238A>G ENSP00000399943.2:n.60+238A>G
ENST00000427987.6:c.95A>G ENSP00000403821.2:p.Asp32Gly
ENST00000430521.2:c.91-74A>G ENSP00000388068.2:n.91-74A>G
ENST00000462048.2:c.-101-74A>G ENSP00000490465.1:n.-101-74A>G
ENST00000465925.6:n.258A>G
ENST00000473163.2:n.341A>G
ENST00000476127.6:n.116A>G
ENST00000476226.6:n.238A>G
ENST00000478594.6:n.244A>G
ENST00000480957.6:n.257A>G
ENST00000485108.6:n.369A>G
ENST00000487589.6:n.152A>G
ENST00000491800.3:n.350A>G
ENST00000493046.6:n.336A>G
ENST00000538581.6:c.95A>G ENSP00000443200.2:p.Asp32Gly
ENST00000635772.1:n.243A>G
ENST00000635808.1:c.239A>G ENSP00000489620.1:p.Asp80Gly
ENST00000635889.1:n.248A>G
ENST00000635936.1:n.231A>G
ENST00000636023.1:c.239A>G ENSP00000489969.1:p.Asp80Gly
ENST00000636070.1:c.91-74A>G ENSP00000490160.1:n.91-74A>G
ENST00000636148.1:n.309A>G
ENST00000636166.1:c.496-551A>G ENSP00000490106.1:n.496-551A>G
ENST00000636199.1:c.239A>G ENSP00000490871.1:p.Asp80Gly
ENST00000636204.1:n.1521A>G
ENST00000636461.1:c.3351A>G
ENST00000636522.1:c.90+238A>G ENSP00000489758.1:n.90+238A>G
ENST00000636587.1:n.471A>G
ENST00000636597.1:c.239A>G ENSP00000490251.1:p.Asp80Gly
ENST00000636725.1:n.229A>G
ENST00000636803.1:n.229A>G
ENST00000636865.1:c.95A>G ENSP00000490601.1:p.Asp32Gly
ENST00000636871.1:n.182A>G
ENST00000636978.1:n.243A>G
ENST00000636991.1:n.262A>G
ENST00000637059.1:c.50A>G ENSP00000490153.1:p.Asp17Gly
ENST00000637088.1:n.3794A>G
ENST00000637114.1:n.231A>G
ENST00000637268.1:n.244A>G
ENST00000637291.1:n.247A>G
ENST00000637442.1:n.1734A>G
ENST00000637455.1:c.50A>G ENSP00000489628.1:p.Asp17Gly
ENST00000637457.1:n.266A>G
ENST00000637682.1:c.239A>G ENSP00000489856.1:p.Asp80Gly
ENST00000637684.1:n.341A>G
ENST00000637821.1:c.91-74A>G ENSP00000490482.1:n.91-74A>G
ENST00000637914.1:n.258A>G
ENST00000637982.1:n.231A>G
ENST00000637994.1:n.249A>G
ENST00000638014.1:c.3020A>G
ENST00000638063.1:c.239A>G ENSP00000489760.1:p.Asp80Gly
ENST00000638079.1:c.*755A>G ENSP00000490120.1:n.*755A>G
ENST00000638092.1:n.229A>G
ENST00000638115.1:c.*2000A>G ENSP00000490296.1:n.*2000A>G
ENST00000273588.7:c.239A>G ENSP00000273588.3:p.Asp80Gly
ENST00000395338.6:c.239A>G ENSP00000378747.2:p.Asp80Gly
ENST00000399379.6:c.91-74A>G ENSP00000399943.1:n.91-74A>G
ENST00000427987.5:c.231A>G
ENST00000430521.1:c.90+238A>G ENSP00000388068.1:n.90+238A>G
ENST00000458307.6:c.239A>G ENSP00000415619.2:p.Asp80Gly
ENST00000462048.1:n.248-74A>G
ENST00000476226.5:n.304A>G
ENST00000478594.5:n.233A>G
ENST00000480957.5:n.247A>G
ENST00000485108.5:n.233A>G
ENST00000487589.5:n.341A>G
ENST00000493046.5:n.92-74A>G
ENST00000495436.5:n.329A>G
ENST00000498571.1:n.237A>G
ENST00000538581.5:c.90+238A>G ENSP00000443200.1:n.90+238A>G
NM_000481.3:c.239A>G , LRG_537t1:c.239A>G NP_000472.2:p.Asp80Gly
NM_001164710.1:c.239A>G NP_001158182.1:p.Asp80Gly
NM_001164711.1:c.90+238A>G NP_001158183.1:n.90+238A>G
NM_001164712.1:c.239A>G NP_001158184.1:p.Asp80Gly
NR_028435.1:n.453A>G
NM_000481.4:c.239A>G MANE Select NP_000472.2:p.Asp80Gly
NM_001164710.2:c.239A>G NP_001158182.1:p.Asp80Gly
NM_001164711.2:c.90+238A>G NP_001158183.1:n.90+238A>G
NM_001164712.2:c.239A>G NP_001158184.1:p.Asp80Gly
NR_028435.2:n.248A>G