Canonical Allele Identifier: CA1363479542

Gene: AMT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49417816A= , CM000665.2:g.49417816A=	GRCh38
NC_000003.11:g.49455249A= , CM000665.1:g.49455249A=	GRCh37
NC_000003.10:g.49430253A=	NCBI36
NG_015986.1:g.9863T= , LRG_537:g.9863T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000273588.9:c.1033+2T= MANE Select	ENSP00000273588.3:n.1033+2T=
ENST00000395338.7:c.1033+2T=	ENSP00000378747.2:n.1033+2T=
ENST00000399379.7:c.765+2T=	ENSP00000399943.2:n.765+2T=
ENST00000427987.6:c.889+2T=	ENSP00000403821.2:n.889+2T=
ENST00000465925.6:n.3035+2T=
ENST00000473163.2:n.3649+2T=
ENST00000476127.6:n.1262+2T=
ENST00000476226.6:n.1454+2T=
ENST00000478594.6:n.1460+2T=
ENST00000493046.6:n.2750-98T=
ENST00000538581.6:c.889+2T=	ENSP00000443200.2:n.889+2T=
ENST00000635772.1:n.1871+2T=
ENST00000635798.1:n.392-98T=
ENST00000635808.1:c.952+2T=	ENSP00000489620.1:n.952+2T=
ENST00000635889.1:n.1526+2T=
ENST00000635907.1:n.592-98T=
ENST00000635936.1:n.1301+2T=
ENST00000636023.1:c.*206+2T=	ENSP00000489969.1:n.*206+2T=
ENST00000636070.1:c.*813+2T=	ENSP00000490160.1:n.*813+2T=
ENST00000636148.1:n.3086+2T=
ENST00000636166.1:c.1270+2T=	ENSP00000490106.1:n.1270+2T=
ENST00000636188.1:c.212+2T=
ENST00000636199.1:c.595+2T=	ENSP00000490871.1:n.595+2T=
ENST00000636204.1:n.2315+2T=
ENST00000636461.1:c.4567+2T=
ENST00000636522.1:c.865+2T=	ENSP00000489758.1:n.865+2T=
ENST00000636587.1:n.1119+2T=
ENST00000636594.1:n.557T=
ENST00000636597.1:c.551-98T=	ENSP00000490251.1:n.551-98T=
ENST00000636725.1:n.1749+2T=
ENST00000636803.1:n.1375+2T=
ENST00000636865.1:c.877+2T=	ENSP00000490601.1:n.877+2T=
ENST00000636871.1:n.1398+2T=
ENST00000636978.1:n.1145+2T=
ENST00000636991.1:n.1478+2T=
ENST00000637059.1:c.485+2T=	ENSP00000490153.1:n.485+2T=
ENST00000637088.1:n.5845+2T=
ENST00000637114.1:n.1133+2T=
ENST00000637268.1:n.1934+2T=
ENST00000637291.1:n.1767+2T=
ENST00000637442.1:n.3254+2T=
ENST00000637455.1:c.844+2T=	ENSP00000489628.1:n.844+2T=
ENST00000637457.1:n.1894+2T=
ENST00000637527.1:n.325+2T=
ENST00000637682.1:c.878-98T=	ENSP00000489856.1:n.878-98T=
ENST00000637684.1:n.1243+2T=
ENST00000637821.1:c.*1229-98T=	ENSP00000490482.1:n.*1229-98T=
ENST00000637914.1:n.2927+2T=
ENST00000637982.1:n.1447+2T=
ENST00000637994.1:n.1573+2T=
ENST00000638014.1:c.3814+2T=
ENST00000638063.1:c.952+2T=	ENSP00000489760.1:n.952+2T=
ENST00000638079.1:c.*1545+2T=	ENSP00000490120.1:n.*1545+2T=
ENST00000638092.1:n.1553+2T=
ENST00000638115.1:c.*2794+2T=	ENSP00000490296.1:n.*2794+2T=
ENST00000273588.7:c.1033+2T=	ENSP00000273588.3:n.1033+2T=
ENST00000395338.6:c.1033+2T=	ENSP00000378747.2:n.1033+2T=
ENST00000399379.6:c.*813+2T=	ENSP00000399943.1:n.*813+2T=
ENST00000427987.5:c.1025+2T=
ENST00000458307.6:c.901+2T=	ENSP00000415619.2:n.901+2T=
ENST00000465925.5:n.2331+2T=
ENST00000473163.1:n.402+2T=
ENST00000476127.5:n.792+2T=
ENST00000476226.5:n.1098+2T=
ENST00000495436.5:n.655-98T=
ENST00000538581.5:c.865+2T=	ENSP00000443200.1:n.865+2T=
NM_000481.3:c.1033+2T= , LRG_537t1:c.1033+2T=	NP_000472.2:n.1033+2T=
NM_001164710.1:c.901+2T=	NP_001158182.1:n.901+2T=
NM_001164711.1:c.865+2T=	NP_001158183.1:n.865+2T=
NM_001164712.1:c.1033+2T=	NP_001158184.1:n.1033+2T=
NR_028435.1:n.1247+2T=
NM_000481.4:c.1033+2T= MANE Select	NP_000472.2:n.1033+2T=
NM_001164710.2:c.901+2T=	NP_001158182.1:n.901+2T=
NM_001164711.2:c.865+2T=	NP_001158183.1:n.865+2T=
NM_001164712.2:c.1033+2T=	NP_001158184.1:n.1033+2T=
NR_028435.2:n.1042+2T=