Canonical Allele Identifier: CA352791307

Gene: AMT

Linked Data

• MyVariant Identifiers: chr3:g.49459680A>C (hg19) ; chr3:g.49422247A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49422247A>C , CM000665.2:g.49422247A>C	GRCh38
NC_000003.11:g.49459680A>C , CM000665.1:g.49459680A>C	GRCh37
NC_000003.10:g.49434684A>C	NCBI36
NG_015986.1:g.5432T>G , LRG_537:g.5432T>G
NG_033046.1:g.12078T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273588.9:c.115T>G MANE Select	ENSP00000273588.3:p.Tyr39Asp
ENST00000395338.7:c.115T>G	ENSP00000378747.2:p.Tyr39Asp
ENST00000399379.7:c.60+114T>G	ENSP00000399943.2:n.60+114T>G
ENST00000427987.6:c.-30T>G	ENSP00000403821.2:n.-30T>G
ENST00000430521.2:c.90+114T>G	ENSP00000388068.2:n.90+114T>G
ENST00000462048.2:c.-102+192T>G	ENSP00000490465.1:n.-102+192T>G
ENST00000465925.6:n.134T>G
ENST00000473163.2:n.217T>G
ENST00000476226.6:n.114T>G
ENST00000478594.6:n.120T>G
ENST00000480957.6:n.133T>G
ENST00000485108.6:n.245T>G
ENST00000487589.6:n.28T>G
ENST00000491800.3:n.226T>G
ENST00000493046.6:n.212T>G
ENST00000538581.6:c.-30T>G	ENSP00000443200.2:n.-30T>G
ENST00000635772.1:n.119T>G
ENST00000635808.1:c.115T>G	ENSP00000489620.1:p.Tyr39Asp
ENST00000635889.1:n.124T>G
ENST00000635936.1:n.107T>G
ENST00000636023.1:c.115T>G	ENSP00000489969.1:p.Tyr39Asp
ENST00000636070.1:c.90+114T>G	ENSP00000490160.1:n.90+114T>G
ENST00000636148.1:n.185T>G
ENST00000636166.1:c.496-675T>G	ENSP00000490106.1:n.496-675T>G
ENST00000636199.1:c.115T>G	ENSP00000490871.1:p.Tyr39Asp
ENST00000636204.1:n.1397T>G
ENST00000636461.1:c.3227T>G
ENST00000636522.1:c.90+114T>G	ENSP00000489758.1:n.90+114T>G
ENST00000636587.1:n.347T>G
ENST00000636597.1:c.115T>G	ENSP00000490251.1:p.Tyr39Asp
ENST00000636725.1:n.105T>G
ENST00000636803.1:n.105T>G
ENST00000636865.1:c.-30T>G	ENSP00000490601.1:n.-30T>G
ENST00000636871.1:n.58T>G
ENST00000636978.1:n.119T>G
ENST00000636991.1:n.138T>G
ENST00000637088.1:n.3670T>G
ENST00000637114.1:n.107T>G
ENST00000637268.1:n.120T>G
ENST00000637291.1:n.123T>G
ENST00000637442.1:n.1610T>G
ENST00000637457.1:n.142T>G
ENST00000637682.1:c.115T>G	ENSP00000489856.1:p.Tyr39Asp
ENST00000637684.1:n.217T>G
ENST00000637821.1:c.90+114T>G	ENSP00000490482.1:n.90+114T>G
ENST00000637914.1:n.134T>G
ENST00000637982.1:n.107T>G
ENST00000637994.1:n.125T>G
ENST00000638014.1:c.2896T>G
ENST00000638063.1:c.115T>G	ENSP00000489760.1:p.Tyr39Asp
ENST00000638079.1:c.*631T>G	ENSP00000490120.1:n.*631T>G
ENST00000638092.1:n.105T>G
ENST00000638115.1:c.*1876T>G	ENSP00000490296.1:n.*1876T>G
ENST00000273588.7:c.115T>G	ENSP00000273588.3:p.Tyr39Asp
ENST00000395338.6:c.115T>G	ENSP00000378747.2:p.Tyr39Asp
ENST00000399379.6:c.90+114T>G	ENSP00000399943.1:n.90+114T>G
ENST00000427987.5:c.107T>G
ENST00000430521.1:c.90+114T>G	ENSP00000388068.1:n.90+114T>G
ENST00000458307.6:c.115T>G	ENSP00000415619.2:p.Tyr39Asp
ENST00000462048.1:n.247+192T>G
ENST00000476226.5:n.180T>G
ENST00000478594.5:n.109T>G
ENST00000480957.5:n.123T>G
ENST00000485108.5:n.109T>G
ENST00000487589.5:n.217T>G
ENST00000493046.5:n.91+114T>G
ENST00000495436.5:n.205T>G
ENST00000498571.1:n.113T>G
ENST00000538581.5:c.90+114T>G	ENSP00000443200.1:n.90+114T>G
NM_000481.3:c.115T>G , LRG_537t1:c.115T>G	NP_000472.2:p.Tyr39Asp
NM_001164710.1:c.115T>G	NP_001158182.1:p.Tyr39Asp
NM_001164711.1:c.90+114T>G	NP_001158183.1:n.90+114T>G
NM_001164712.1:c.115T>G	NP_001158184.1:p.Tyr39Asp
NR_028435.1:n.329T>G
NM_000481.4:c.115T>G MANE Select	NP_000472.2:p.Tyr39Asp
NM_001164710.2:c.115T>G	NP_001158182.1:p.Tyr39Asp
NM_001164711.2:c.90+114T>G	NP_001158183.1:n.90+114T>G
NM_001164712.2:c.115T>G	NP_001158184.1:p.Tyr39Asp
NR_028435.2:n.124T>G