Canonical Allele Identifier: CA263589
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 56240
ClinVar RCV Id: RCV000049652
dbSNP Id: rs386833691

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49417881_49417883del , CM000665.2:g.49417881_49417883del GRCh38
NC_000003.11:g.49455314_49455316del , CM000665.1:g.49455314_49455316del GRCh37
NC_000003.10:g.49430318_49430320del NCBI36
NG_015986.1:g.9798_9800del , LRG_537:g.9798_9800del

Transcript Alleles

HGVS Amino-acid change
ENST00000273588.9:c.970_972del MANE Select ENSP00000273588.3:p.Met324del
ENST00000395338.7:c.970_972del ENSP00000378747.2:p.Met324del
ENST00000399379.7:c.702_704del ENSP00000399943.2:n.702_704del
ENST00000427987.6:c.826_828del ENSP00000403821.2:p.Met276del
ENST00000465925.6:n.2972_2974del
ENST00000473163.2:n.3586_3588del
ENST00000476127.6:n.1199_1201del
ENST00000476226.6:n.1391_1393del
ENST00000478594.6:n.1397_1399del
ENST00000493046.6:n.2750-163_2750-161del
ENST00000538581.6:c.826_828del ENSP00000443200.2:p.Met276del
ENST00000635772.1:n.1808_1810del
ENST00000635798.1:n.392-163_392-161del
ENST00000635808.1:c.889_891del ENSP00000489620.1:p.Met297del
ENST00000635889.1:n.1463_1465del
ENST00000635907.1:n.592-163_592-161del
ENST00000635936.1:n.1238_1240del
ENST00000636023.1:c.*143_*145del ENSP00000489969.1:n.*143_*145del
ENST00000636070.1:c.*750_*752del ENSP00000490160.1:n.*750_*752del
ENST00000636148.1:n.3023_3025del
ENST00000636166.1:c.1207_1209del ENSP00000490106.1:p.Met403del
ENST00000636188.1:c.149_151del
ENST00000636199.1:c.532_534del ENSP00000490871.1:p.Met178del
ENST00000636204.1:n.2252_2254del
ENST00000636461.1:c.4504_4506del
ENST00000636522.1:c.802_804del ENSP00000489758.1:p.Met268del
ENST00000636587.1:n.1056_1058del
ENST00000636594.1:n.492_494del
ENST00000636597.1:c.551-163_551-161del ENSP00000490251.1:n.551-163_551-161del
ENST00000636725.1:n.1686_1688del
ENST00000636803.1:n.1312_1314del
ENST00000636865.1:c.814_816del ENSP00000490601.1:p.Met272del
ENST00000636871.1:n.1335_1337del
ENST00000636978.1:n.1082_1084del
ENST00000636991.1:n.1415_1417del
ENST00000637059.1:c.422_424del ENSP00000490153.1:n.422_424del
ENST00000637088.1:n.5782_5784del
ENST00000637114.1:n.1070_1072del
ENST00000637268.1:n.1871_1873del
ENST00000637291.1:n.1704_1706del
ENST00000637442.1:n.3191_3193del
ENST00000637455.1:c.781_783del ENSP00000489628.1:p.Met261del
ENST00000637457.1:n.1831_1833del
ENST00000637527.1:n.262_264del
ENST00000637682.1:c.878-163_878-161del ENSP00000489856.1:n.878-163_878-161del
ENST00000637684.1:n.1180_1182del
ENST00000637821.1:c.*1228+52_*1228+54del ENSP00000490482.1:n.*1228+52_*1228+54del
ENST00000637914.1:n.2864_2866del
ENST00000637982.1:n.1384_1386del
ENST00000637994.1:n.1510_1512del
ENST00000638014.1:c.3751_3753del
ENST00000638063.1:c.889_891del ENSP00000489760.1:p.Met297del
ENST00000638079.1:c.*1482_*1484del ENSP00000490120.1:n.*1482_*1484del
ENST00000638092.1:n.1490_1492del
ENST00000638115.1:c.*2731_*2733del ENSP00000490296.1:n.*2731_*2733del
ENST00000273588.7:c.970_972del ENSP00000273588.3:p.Met324del
ENST00000395338.6:c.970_972del ENSP00000378747.2:p.Met324del
ENST00000399379.6:c.*750_*752del ENSP00000399943.1:n.*750_*752del
ENST00000427987.5:c.962_964del
ENST00000458307.6:c.838_840del ENSP00000415619.2:p.Met280del
ENST00000465925.5:n.2268_2270del
ENST00000473163.1:n.339_341del
ENST00000476127.5:n.729_731del
ENST00000476226.5:n.1035_1037del
ENST00000495436.5:n.655-163_655-161del
ENST00000538581.5:c.802_804del ENSP00000443200.1:p.Met268del
NM_000481.3:c.970_972del , LRG_537t1:c.970_972del NP_000472.2:p.Met324del
NM_001164710.1:c.838_840del NP_001158182.1:p.Met280del
NM_001164711.1:c.802_804del NP_001158183.1:p.Met268del
NM_001164712.1:c.970_972del NP_001158184.1:p.Met324del
NR_028435.1:n.1184_1186del
NM_000481.4:c.970_972del MANE Select NP_000472.2:p.Met324del
NM_001164710.2:c.838_840del NP_001158182.1:p.Met280del
NM_001164711.2:c.802_804del NP_001158183.1:p.Met268del
NM_001164712.2:c.970_972del NP_001158184.1:p.Met324del
NR_028435.2:n.979_981del