Canonical Allele Identifier: CA352791103
Gene: AMT HGNC NCBI

Linked Data

dbSNP Id: rs776333905

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49422149G>C , CM000665.2:g.49422149G>C GRCh38
NC_000003.11:g.49459582G>C , CM000665.1:g.49459582G>C GRCh37
NC_000003.10:g.49434586G>C NCBI36
NG_015986.1:g.5530C>G , LRG_537:g.5530C>G
NG_033046.1:g.12176C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000273588.9:c.213C>G MANE Select ENSP00000273588.3:p.His71Gln
ENST00000395338.7:c.213C>G ENSP00000378747.2:p.His71Gln
ENST00000399379.7:c.60+212C>G ENSP00000399943.2:n.60+212C>G
ENST00000427987.6:c.69C>G ENSP00000403821.2:p.His23Gln
ENST00000430521.2:c.91-100C>G ENSP00000388068.2:n.91-100C>G
ENST00000462048.2:c.-101-100C>G ENSP00000490465.1:n.-101-100C>G
ENST00000465925.6:n.232C>G
ENST00000473163.2:n.315C>G
ENST00000476127.6:n.90C>G
ENST00000476226.6:n.212C>G
ENST00000478594.6:n.218C>G
ENST00000480957.6:n.231C>G
ENST00000485108.6:n.343C>G
ENST00000487589.6:n.126C>G
ENST00000491800.3:n.324C>G
ENST00000493046.6:n.310C>G
ENST00000538581.6:c.69C>G ENSP00000443200.2:p.His23Gln
ENST00000635772.1:n.217C>G
ENST00000635808.1:c.213C>G ENSP00000489620.1:p.His71Gln
ENST00000635889.1:n.222C>G
ENST00000635936.1:n.205C>G
ENST00000636023.1:c.213C>G ENSP00000489969.1:p.His71Gln
ENST00000636070.1:c.91-100C>G ENSP00000490160.1:n.91-100C>G
ENST00000636148.1:n.283C>G
ENST00000636166.1:c.496-577C>G ENSP00000490106.1:n.496-577C>G
ENST00000636199.1:c.213C>G ENSP00000490871.1:p.His71Gln
ENST00000636204.1:n.1495C>G
ENST00000636461.1:c.3325C>G
ENST00000636522.1:c.90+212C>G ENSP00000489758.1:n.90+212C>G
ENST00000636587.1:n.445C>G
ENST00000636597.1:c.213C>G ENSP00000490251.1:p.His71Gln
ENST00000636725.1:n.203C>G
ENST00000636803.1:n.203C>G
ENST00000636865.1:c.69C>G ENSP00000490601.1:p.His23Gln
ENST00000636871.1:n.156C>G
ENST00000636978.1:n.217C>G
ENST00000636991.1:n.236C>G
ENST00000637059.1:c.24C>G ENSP00000490153.1:p.His8Gln
ENST00000637088.1:n.3768C>G
ENST00000637114.1:n.205C>G
ENST00000637268.1:n.218C>G
ENST00000637291.1:n.221C>G
ENST00000637442.1:n.1708C>G
ENST00000637455.1:c.24C>G ENSP00000489628.1:p.His8Gln
ENST00000637457.1:n.240C>G
ENST00000637682.1:c.213C>G ENSP00000489856.1:p.His71Gln
ENST00000637684.1:n.315C>G
ENST00000637821.1:c.91-100C>G ENSP00000490482.1:n.91-100C>G
ENST00000637914.1:n.232C>G
ENST00000637982.1:n.205C>G
ENST00000637994.1:n.223C>G
ENST00000638014.1:c.2994C>G
ENST00000638063.1:c.213C>G ENSP00000489760.1:p.His71Gln
ENST00000638079.1:c.*729C>G ENSP00000490120.1:n.*729C>G
ENST00000638092.1:n.203C>G
ENST00000638115.1:c.*1974C>G ENSP00000490296.1:n.*1974C>G
ENST00000273588.7:c.213C>G ENSP00000273588.3:p.His71Gln
ENST00000395338.6:c.213C>G ENSP00000378747.2:p.His71Gln
ENST00000399379.6:c.91-100C>G ENSP00000399943.1:n.91-100C>G
ENST00000427987.5:c.205C>G
ENST00000430521.1:c.90+212C>G ENSP00000388068.1:n.90+212C>G
ENST00000458307.6:c.213C>G ENSP00000415619.2:p.His71Gln
ENST00000462048.1:n.248-100C>G
ENST00000476226.5:n.278C>G
ENST00000478594.5:n.207C>G
ENST00000480957.5:n.221C>G
ENST00000485108.5:n.207C>G
ENST00000487589.5:n.315C>G
ENST00000493046.5:n.92-100C>G
ENST00000495436.5:n.303C>G
ENST00000498571.1:n.211C>G
ENST00000538581.5:c.90+212C>G ENSP00000443200.1:n.90+212C>G
NM_000481.3:c.213C>G , LRG_537t1:c.213C>G NP_000472.2:p.His71Gln
NM_001164710.1:c.213C>G NP_001158182.1:p.His71Gln
NM_001164711.1:c.90+212C>G NP_001158183.1:n.90+212C>G
NM_001164712.1:c.213C>G NP_001158184.1:p.His71Gln
NR_028435.1:n.427C>G
NM_000481.4:c.213C>G MANE Select NP_000472.2:p.His71Gln
NM_001164710.2:c.213C>G NP_001158182.1:p.His71Gln
NM_001164711.2:c.90+212C>G NP_001158183.1:n.90+212C>G
NM_001164712.2:c.213C>G NP_001158184.1:p.His71Gln
NR_028435.2:n.222C>G