Canonical Allele Identifier: CA433648017

Gene: AMT

Linked Data

• MyVariant Identifiers: chr3:g.49459609C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49422176C>A , CM000665.2:g.49422176C>A	GRCh38
NC_000003.11:g.49459609C>A , CM000665.1:g.49459609C>A	GRCh37
NC_000003.10:g.49434613C>A	NCBI36
NG_015986.1:g.5503G>T , LRG_537:g.5503G>T
NG_033046.1:g.12149G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273588.9:c.186G>T MANE Select	ENSP00000273588.3:p.Arg62=
ENST00000395338.7:c.186G>T	ENSP00000378747.2:p.Arg62=
ENST00000399379.7:c.60+185G>T	ENSP00000399943.2:n.60+185G>T
ENST00000427987.6:c.42G>T	ENSP00000403821.2:p.Arg14=
ENST00000430521.2:c.91-127G>T	ENSP00000388068.2:n.91-127G>T
ENST00000462048.2:c.-101-127G>T	ENSP00000490465.1:n.-101-127G>T
ENST00000465925.6:n.205G>T
ENST00000473163.2:n.288G>T
ENST00000476127.6:n.63G>T
ENST00000476226.6:n.185G>T
ENST00000478594.6:n.191G>T
ENST00000480957.6:n.204G>T
ENST00000485108.6:n.316G>T
ENST00000487589.6:n.99G>T
ENST00000491800.3:n.297G>T
ENST00000493046.6:n.283G>T
ENST00000538581.6:c.42G>T	ENSP00000443200.2:p.Arg14=
ENST00000635772.1:n.190G>T
ENST00000635808.1:c.186G>T	ENSP00000489620.1:p.Arg62=
ENST00000635889.1:n.195G>T
ENST00000635936.1:n.178G>T
ENST00000636023.1:c.186G>T	ENSP00000489969.1:p.Arg62=
ENST00000636070.1:c.91-127G>T	ENSP00000490160.1:n.91-127G>T
ENST00000636148.1:n.256G>T
ENST00000636166.1:c.496-604G>T	ENSP00000490106.1:n.496-604G>T
ENST00000636199.1:c.186G>T	ENSP00000490871.1:p.Arg62=
ENST00000636204.1:n.1468G>T
ENST00000636461.1:c.3298G>T
ENST00000636522.1:c.90+185G>T	ENSP00000489758.1:n.90+185G>T
ENST00000636587.1:n.418G>T
ENST00000636597.1:c.186G>T	ENSP00000490251.1:p.Arg62=
ENST00000636725.1:n.176G>T
ENST00000636803.1:n.176G>T
ENST00000636865.1:c.42G>T	ENSP00000490601.1:p.Arg14=
ENST00000636871.1:n.129G>T
ENST00000636978.1:n.190G>T
ENST00000636991.1:n.209G>T
ENST00000637088.1:n.3741G>T
ENST00000637114.1:n.178G>T
ENST00000637268.1:n.191G>T
ENST00000637291.1:n.194G>T
ENST00000637442.1:n.1681G>T
ENST00000637457.1:n.213G>T
ENST00000637682.1:c.186G>T	ENSP00000489856.1:p.Arg62=
ENST00000637684.1:n.288G>T
ENST00000637821.1:c.91-127G>T	ENSP00000490482.1:n.91-127G>T
ENST00000637914.1:n.205G>T
ENST00000637982.1:n.178G>T
ENST00000637994.1:n.196G>T
ENST00000638014.1:c.2967G>T
ENST00000638063.1:c.186G>T	ENSP00000489760.1:p.Arg62=
ENST00000638079.1:c.*702G>T	ENSP00000490120.1:n.*702G>T
ENST00000638092.1:n.176G>T
ENST00000638115.1:c.*1947G>T	ENSP00000490296.1:n.*1947G>T
ENST00000273588.7:c.186G>T	ENSP00000273588.3:p.Arg62=
ENST00000395338.6:c.186G>T	ENSP00000378747.2:p.Arg62=
ENST00000399379.6:c.91-127G>T	ENSP00000399943.1:n.91-127G>T
ENST00000427987.5:c.178G>T
ENST00000430521.1:c.90+185G>T	ENSP00000388068.1:n.90+185G>T
ENST00000458307.6:c.186G>T	ENSP00000415619.2:p.Arg62=
ENST00000462048.1:n.248-127G>T
ENST00000476226.5:n.251G>T
ENST00000478594.5:n.180G>T
ENST00000480957.5:n.194G>T
ENST00000485108.5:n.180G>T
ENST00000487589.5:n.288G>T
ENST00000493046.5:n.92-127G>T
ENST00000495436.5:n.276G>T
ENST00000498571.1:n.184G>T
ENST00000538581.5:c.90+185G>T	ENSP00000443200.1:n.90+185G>T
NM_000481.3:c.186G>T , LRG_537t1:c.186G>T	NP_000472.2:p.Arg62=
NM_001164710.1:c.186G>T	NP_001158182.1:p.Arg62=
NM_001164711.1:c.90+185G>T	NP_001158183.1:n.90+185G>T
NM_001164712.1:c.186G>T	NP_001158184.1:p.Arg62=
NR_028435.1:n.400G>T
NM_000481.4:c.186G>T MANE Select	NP_000472.2:p.Arg62=
NM_001164710.2:c.186G>T	NP_001158182.1:p.Arg62=
NM_001164711.2:c.90+185G>T	NP_001158183.1:n.90+185G>T
NM_001164712.2:c.186G>T	NP_001158184.1:p.Arg62=
NR_028435.2:n.195G>T