Canonical Allele Identifier: CA2841602744

Gene: AMT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49417984A>G , CM000665.2:g.49417984A>G	GRCh38
NC_000003.11:g.49455417A>G , CM000665.1:g.49455417A>G	GRCh37
NC_000003.10:g.49430421A>G	NCBI36
NG_015986.1:g.9695T>C , LRG_537:g.9695T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273588.9:c.878-11T>C MANE Select	ENSP00000273588.3:n.878-11T>C
ENST00000395338.7:c.878-11T>C	ENSP00000378747.2:n.878-11T>C
ENST00000399379.7:c.610-11T>C	ENSP00000399943.2:n.610-11T>C
ENST00000427987.6:c.734-11T>C	ENSP00000403821.2:n.734-11T>C
ENST00000465925.6:n.2880-11T>C
ENST00000473163.2:n.3494-11T>C
ENST00000476127.6:n.1107-11T>C
ENST00000476226.6:n.1299-11T>C
ENST00000478594.6:n.1305-11T>C
ENST00000493046.6:n.2750-266T>C
ENST00000538581.6:c.734-11T>C	ENSP00000443200.2:n.734-11T>C
ENST00000635772.1:n.1716-11T>C
ENST00000635798.1:n.392-266T>C
ENST00000635808.1:c.797-11T>C	ENSP00000489620.1:n.797-11T>C
ENST00000635889.1:n.1371-11T>C
ENST00000635907.1:n.592-266T>C
ENST00000635936.1:n.1146-11T>C
ENST00000636023.1:c.*51-11T>C	ENSP00000489969.1:n.*51-11T>C
ENST00000636070.1:c.*658-11T>C	ENSP00000490160.1:n.*658-11T>C
ENST00000636148.1:n.2931-11T>C
ENST00000636166.1:c.1115-11T>C	ENSP00000490106.1:n.1115-11T>C
ENST00000636188.1:c.57-11T>C
ENST00000636199.1:c.440-11T>C	ENSP00000490871.1:n.440-11T>C
ENST00000636204.1:n.2160-11T>C
ENST00000636461.1:c.4412-11T>C
ENST00000636522.1:c.710-11T>C	ENSP00000489758.1:n.710-11T>C
ENST00000636587.1:n.964-11T>C
ENST00000636594.1:n.389T>C
ENST00000636597.1:c.551-266T>C	ENSP00000490251.1:n.551-266T>C
ENST00000636725.1:n.1594-11T>C
ENST00000636803.1:n.1220-11T>C
ENST00000636865.1:c.722-11T>C	ENSP00000490601.1:n.722-11T>C
ENST00000636871.1:n.1243-11T>C
ENST00000636978.1:n.990-11T>C
ENST00000636991.1:n.1323-11T>C
ENST00000637059.1:c.330-11T>C	ENSP00000490153.1:n.330-11T>C
ENST00000637088.1:n.5690-11T>C
ENST00000637114.1:n.978-11T>C
ENST00000637268.1:n.1779-11T>C
ENST00000637291.1:n.1612-11T>C
ENST00000637442.1:n.3099-11T>C
ENST00000637455.1:c.689-11T>C	ENSP00000489628.1:n.689-11T>C
ENST00000637457.1:n.1739-11T>C
ENST00000637527.1:n.159T>C
ENST00000637682.1:c.878-266T>C	ENSP00000489856.1:n.878-266T>C
ENST00000637684.1:n.1088-11T>C
ENST00000637821.1:c.*1188-11T>C	ENSP00000490482.1:n.*1188-11T>C
ENST00000637914.1:n.2772-11T>C
ENST00000637982.1:n.1292-11T>C
ENST00000637994.1:n.1418-11T>C
ENST00000638014.1:c.3659-11T>C
ENST00000638063.1:c.797-11T>C	ENSP00000489760.1:n.797-11T>C
ENST00000638079.1:c.*1390-11T>C	ENSP00000490120.1:n.*1390-11T>C
ENST00000638092.1:n.1398-11T>C
ENST00000638115.1:c.*2639-11T>C	ENSP00000490296.1:n.*2639-11T>C
ENST00000273588.7:c.878-11T>C	ENSP00000273588.3:n.878-11T>C
ENST00000395338.6:c.878-11T>C	ENSP00000378747.2:n.878-11T>C
ENST00000399379.6:c.*658-11T>C	ENSP00000399943.1:n.*658-11T>C
ENST00000427987.5:c.870-11T>C
ENST00000430521.1:c.710-11T>C	ENSP00000388068.1:n.710-11T>C
ENST00000458307.6:c.746-11T>C	ENSP00000415619.2:n.746-11T>C
ENST00000465925.5:n.2176-11T>C
ENST00000473163.1:n.247-11T>C
ENST00000476127.5:n.637-11T>C
ENST00000476226.5:n.943-11T>C
ENST00000495436.5:n.655-266T>C
ENST00000538581.5:c.710-11T>C	ENSP00000443200.1:n.710-11T>C
NM_000481.3:c.878-11T>C , LRG_537t1:c.878-11T>C	NP_000472.2:n.878-11T>C
NM_001164710.1:c.746-11T>C	NP_001158182.1:n.746-11T>C
NM_001164711.1:c.710-11T>C	NP_001158183.1:n.710-11T>C
NM_001164712.1:c.878-11T>C	NP_001158184.1:n.878-11T>C
NR_028435.1:n.1092-11T>C
NM_000481.4:c.878-11T>C MANE Select	NP_000472.2:n.878-11T>C
NM_001164710.2:c.746-11T>C	NP_001158182.1:n.746-11T>C
NM_001164711.2:c.710-11T>C	NP_001158183.1:n.710-11T>C
NM_001164712.2:c.878-11T>C	NP_001158184.1:n.878-11T>C
NR_028435.2:n.887-11T>C