Canonical Allele Identifier: CA433648040

Gene: AMT

Linked Data

• ClinVar Variation Id: 1089212
• ClinVar RCV Id: RCV001407972
• dbSNP Id: rs768510463
• MyVariant Identifiers: chr3:g.49459642C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49422209C>A , CM000665.2:g.49422209C>A	GRCh38
NC_000003.11:g.49459642C>A , CM000665.1:g.49459642C>A	GRCh37
NC_000003.10:g.49434646C>A	NCBI36
NG_015986.1:g.5470G>T , LRG_537:g.5470G>T
NG_033046.1:g.12116G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273588.9:c.153G>T MANE Select	ENSP00000273588.3:p.Ala51=
ENST00000395338.7:c.153G>T	ENSP00000378747.2:p.Ala51=
ENST00000399379.7:c.60+152G>T	ENSP00000399943.2:n.60+152G>T
ENST00000427987.6:c.9G>T	ENSP00000403821.2:p.Ala3=
ENST00000430521.2:c.90+152G>T	ENSP00000388068.2:n.90+152G>T
ENST00000462048.2:c.-101-160G>T	ENSP00000490465.1:n.-101-160G>T
ENST00000465925.6:n.172G>T
ENST00000473163.2:n.255G>T
ENST00000476127.6:n.30G>T
ENST00000476226.6:n.152G>T
ENST00000478594.6:n.158G>T
ENST00000480957.6:n.171G>T
ENST00000485108.6:n.283G>T
ENST00000487589.6:n.66G>T
ENST00000491800.3:n.264G>T
ENST00000493046.6:n.250G>T
ENST00000538581.6:c.9G>T	ENSP00000443200.2:p.Ala3=
ENST00000635772.1:n.157G>T
ENST00000635808.1:c.153G>T	ENSP00000489620.1:p.Ala51=
ENST00000635889.1:n.162G>T
ENST00000635936.1:n.145G>T
ENST00000636023.1:c.153G>T	ENSP00000489969.1:p.Ala51=
ENST00000636070.1:c.90+152G>T	ENSP00000490160.1:n.90+152G>T
ENST00000636148.1:n.223G>T
ENST00000636166.1:c.496-637G>T	ENSP00000490106.1:n.496-637G>T
ENST00000636199.1:c.153G>T	ENSP00000490871.1:p.Ala51=
ENST00000636204.1:n.1435G>T
ENST00000636461.1:c.3265G>T
ENST00000636522.1:c.90+152G>T	ENSP00000489758.1:n.90+152G>T
ENST00000636587.1:n.385G>T
ENST00000636597.1:c.153G>T	ENSP00000490251.1:p.Ala51=
ENST00000636725.1:n.143G>T
ENST00000636803.1:n.143G>T
ENST00000636865.1:c.9G>T	ENSP00000490601.1:p.Ala3=
ENST00000636871.1:n.96G>T
ENST00000636978.1:n.157G>T
ENST00000636991.1:n.176G>T
ENST00000637088.1:n.3708G>T
ENST00000637114.1:n.145G>T
ENST00000637268.1:n.158G>T
ENST00000637291.1:n.161G>T
ENST00000637442.1:n.1648G>T
ENST00000637457.1:n.180G>T
ENST00000637682.1:c.153G>T	ENSP00000489856.1:p.Ala51=
ENST00000637684.1:n.255G>T
ENST00000637821.1:c.90+152G>T	ENSP00000490482.1:n.90+152G>T
ENST00000637914.1:n.172G>T
ENST00000637982.1:n.145G>T
ENST00000637994.1:n.163G>T
ENST00000638014.1:c.2934G>T
ENST00000638063.1:c.153G>T	ENSP00000489760.1:p.Ala51=
ENST00000638079.1:c.*669G>T	ENSP00000490120.1:n.*669G>T
ENST00000638092.1:n.143G>T
ENST00000638115.1:c.*1914G>T	ENSP00000490296.1:n.*1914G>T
ENST00000273588.7:c.153G>T	ENSP00000273588.3:p.Ala51=
ENST00000395338.6:c.153G>T	ENSP00000378747.2:p.Ala51=
ENST00000399379.6:c.90+152G>T	ENSP00000399943.1:n.90+152G>T
ENST00000427987.5:c.145G>T
ENST00000430521.1:c.90+152G>T	ENSP00000388068.1:n.90+152G>T
ENST00000458307.6:c.153G>T	ENSP00000415619.2:p.Ala51=
ENST00000462048.1:n.248-160G>T
ENST00000476226.5:n.218G>T
ENST00000478594.5:n.147G>T
ENST00000480957.5:n.161G>T
ENST00000485108.5:n.147G>T
ENST00000487589.5:n.255G>T
ENST00000493046.5:n.91+152G>T
ENST00000495436.5:n.243G>T
ENST00000498571.1:n.151G>T
ENST00000538581.5:c.90+152G>T	ENSP00000443200.1:n.90+152G>T
NM_000481.3:c.153G>T , LRG_537t1:c.153G>T	NP_000472.2:p.Ala51=
NM_001164710.1:c.153G>T	NP_001158182.1:p.Ala51=
NM_001164711.1:c.90+152G>T	NP_001158183.1:n.90+152G>T
NM_001164712.1:c.153G>T	NP_001158184.1:p.Ala51=
NR_028435.1:n.367G>T
NM_000481.4:c.153G>T MANE Select	NP_000472.2:p.Ala51=
NM_001164710.2:c.153G>T	NP_001158182.1:p.Ala51=
NM_001164711.2:c.90+152G>T	NP_001158183.1:n.90+152G>T
NM_001164712.2:c.153G>T	NP_001158184.1:p.Ala51=
NR_028435.2:n.162G>T