Canonical Allele Identifier: CA352791259

Gene: AMT

Linked Data

• gnomAD v4: 3-49422225-C-T
• MyVariant Identifiers: chr3:g.49459658C>T (hg19) ; chr3:g.49422225C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49422225C>T , CM000665.2:g.49422225C>T	GRCh38
NC_000003.11:g.49459658C>T , CM000665.1:g.49459658C>T	GRCh37
NC_000003.10:g.49434662C>T	NCBI36
NG_015986.1:g.5454G>A , LRG_537:g.5454G>A
NG_033046.1:g.12100G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273588.9:c.137G>A MANE Select	ENSP00000273588.3:p.Gly46Asp
ENST00000395338.7:c.137G>A	ENSP00000378747.2:p.Gly46Asp
ENST00000399379.7:c.60+136G>A	ENSP00000399943.2:n.60+136G>A
ENST00000427987.6:c.-8G>A	ENSP00000403821.2:n.-8G>A
ENST00000430521.2:c.90+136G>A	ENSP00000388068.2:n.90+136G>A
ENST00000462048.2:c.-101-176G>A	ENSP00000490465.1:n.-101-176G>A
ENST00000465925.6:n.156G>A
ENST00000473163.2:n.239G>A
ENST00000476127.6:n.14G>A
ENST00000476226.6:n.136G>A
ENST00000478594.6:n.142G>A
ENST00000480957.6:n.155G>A
ENST00000485108.6:n.267G>A
ENST00000487589.6:n.50G>A
ENST00000491800.3:n.248G>A
ENST00000493046.6:n.234G>A
ENST00000538581.6:c.-8G>A	ENSP00000443200.2:n.-8G>A
ENST00000635772.1:n.141G>A
ENST00000635808.1:c.137G>A	ENSP00000489620.1:p.Gly46Asp
ENST00000635889.1:n.146G>A
ENST00000635936.1:n.129G>A
ENST00000636023.1:c.137G>A	ENSP00000489969.1:p.Gly46Asp
ENST00000636070.1:c.90+136G>A	ENSP00000490160.1:n.90+136G>A
ENST00000636148.1:n.207G>A
ENST00000636166.1:c.496-653G>A	ENSP00000490106.1:n.496-653G>A
ENST00000636199.1:c.137G>A	ENSP00000490871.1:p.Gly46Asp
ENST00000636204.1:n.1419G>A
ENST00000636461.1:c.3249G>A
ENST00000636522.1:c.90+136G>A	ENSP00000489758.1:n.90+136G>A
ENST00000636587.1:n.369G>A
ENST00000636597.1:c.137G>A	ENSP00000490251.1:p.Gly46Asp
ENST00000636725.1:n.127G>A
ENST00000636803.1:n.127G>A
ENST00000636865.1:c.-8G>A	ENSP00000490601.1:n.-8G>A
ENST00000636871.1:n.80G>A
ENST00000636978.1:n.141G>A
ENST00000636991.1:n.160G>A
ENST00000637088.1:n.3692G>A
ENST00000637114.1:n.129G>A
ENST00000637268.1:n.142G>A
ENST00000637291.1:n.145G>A
ENST00000637442.1:n.1632G>A
ENST00000637457.1:n.164G>A
ENST00000637682.1:c.137G>A	ENSP00000489856.1:p.Gly46Asp
ENST00000637684.1:n.239G>A
ENST00000637821.1:c.90+136G>A	ENSP00000490482.1:n.90+136G>A
ENST00000637914.1:n.156G>A
ENST00000637982.1:n.129G>A
ENST00000637994.1:n.147G>A
ENST00000638014.1:c.2918G>A
ENST00000638063.1:c.137G>A	ENSP00000489760.1:p.Gly46Asp
ENST00000638079.1:c.*653G>A	ENSP00000490120.1:n.*653G>A
ENST00000638092.1:n.127G>A
ENST00000638115.1:c.*1898G>A	ENSP00000490296.1:n.*1898G>A
ENST00000273588.7:c.137G>A	ENSP00000273588.3:p.Gly46Asp
ENST00000395338.6:c.137G>A	ENSP00000378747.2:p.Gly46Asp
ENST00000399379.6:c.90+136G>A	ENSP00000399943.1:n.90+136G>A
ENST00000427987.5:c.129G>A
ENST00000430521.1:c.90+136G>A	ENSP00000388068.1:n.90+136G>A
ENST00000458307.6:c.137G>A	ENSP00000415619.2:p.Gly46Asp
ENST00000462048.1:n.248-176G>A
ENST00000476226.5:n.202G>A
ENST00000478594.5:n.131G>A
ENST00000480957.5:n.145G>A
ENST00000485108.5:n.131G>A
ENST00000487589.5:n.239G>A
ENST00000493046.5:n.91+136G>A
ENST00000495436.5:n.227G>A
ENST00000498571.1:n.135G>A
ENST00000538581.5:c.90+136G>A	ENSP00000443200.1:n.90+136G>A
NM_000481.3:c.137G>A , LRG_537t1:c.137G>A	NP_000472.2:p.Gly46Asp
NM_001164710.1:c.137G>A	NP_001158182.1:p.Gly46Asp
NM_001164711.1:c.90+136G>A	NP_001158183.1:n.90+136G>A
NM_001164712.1:c.137G>A	NP_001158184.1:p.Gly46Asp
NR_028435.1:n.351G>A
NM_000481.4:c.137G>A MANE Select	NP_000472.2:p.Gly46Asp
NM_001164710.2:c.137G>A	NP_001158182.1:p.Gly46Asp
NM_001164711.2:c.90+136G>A	NP_001158183.1:n.90+136G>A
NM_001164712.2:c.137G>A	NP_001158184.1:p.Gly46Asp
NR_028435.2:n.146G>A