Canonical Allele Identifier: CA2619052891
Gene: AMHR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429745_53429746del , CM000674.2:g.53429745_53429746del GRCh38
NC_000012.11:g.53823529_53823530del , CM000674.1:g.53823529_53823530del GRCh37
NC_000012.10:g.52109796_52109797del NCBI36
NG_015981.1:g.10891_10892del

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1141-86_1141-85del MANE Select ENSP00000257863.3:n.1141-86_1141-85del
ENST00000257863.8:c.1141-86_1141-85del ENSP00000257863.3:n.1141-86_1141-85del
ENST00000379791.7:c.1140+120_1140+121del ENSP00000369117.3:n.1140+120_1140+121del
ENST00000550311.5:c.1141-86_1141-85del ENSP00000446661.1:n.1141-86_1141-85del
ENST00000550839.1:c.232-86_232-85del ENSP00000455338.1:n.232-86_232-85del
ENST00000552233.5:n.643_644del
NM_001164690.1:c.1141-86_1141-85del NP_001158162.1:n.1141-86_1141-85del
NM_001164691.1:c.1140+120_1140+121del NP_001158163.1:n.1140+120_1140+121del
NM_020547.2:c.1141-86_1141-85del NP_065434.1:n.1141-86_1141-85del
XM_011538173.1:c.1201-86_1201-85del XP_011536475.1:n.1201-86_1201-85del
XM_011538174.1:c.1198-86_1198-85del XP_011536476.1:n.1198-86_1198-85del
XM_011538175.1:c.1183-86_1183-85del XP_011536477.1:n.1183-86_1183-85del
XM_011538176.1:c.1144-86_1144-85del XP_011536478.1:n.1144-86_1144-85del
XM_011538177.1:c.1123-86_1123-85del XP_011536479.1:n.1123-86_1123-85del
XM_011538178.1:c.982-86_982-85del XP_011536480.1:n.982-86_982-85del
XM_011538179.1:c.1200+120_1200+121del XP_011536481.1:n.1200+120_1200+121del
XM_011538180.1:c.868-86_868-85del XP_011536482.1:n.868-86_868-85del
XM_011538181.1:c.865-86_865-85del XP_011536483.1:n.865-86_865-85del
XM_011538182.1:c.790-86_790-85del XP_011536484.1:n.790-86_790-85del
XM_011538183.1:c.1200+120_1200+121del XP_011536485.1:n.1200+120_1200+121del
XM_011538184.1:c.1220+100_1220+101del XP_011536486.1:n.1220+100_1220+101del
XM_011538185.1:c.856-1432_856-1431del XP_011536487.1:n.856-1432_856-1431del
XM_011538186.1:c.316-86_316-85del XP_011536488.1:n.316-86_316-85del
NM_001164690.2:c.1141-86_1141-85del NP_001158162.1:n.1141-86_1141-85del
NM_001164691.2:c.1140+120_1140+121del NP_001158163.1:n.1140+120_1140+121del
NM_020547.3:c.1141-86_1141-85del MANE Select NP_065434.1:n.1141-86_1141-85del
XM_011538183.2:c.1200+120_1200+121del XP_011536485.1:n.1200+120_1200+121del
XM_011538184.2:c.1220+100_1220+101del XP_011536486.1:n.1220+100_1220+101del
XM_011538186.3:c.316-86_316-85del XP_011536488.1:n.316-86_316-85del
XM_017019179.2:c.1201-86_1201-85del XP_016874668.1:n.1201-86_1201-85del
XM_024448938.1:c.1143+120_1143+121del XP_024304706.1:n.1143+120_1143+121del
XR_002957309.1:n.1109-86_1109-85del
XR_002957310.1:n.1108+120_1108+121del
XR_002957311.1:n.1109-86_1109-85del
XR_002957312.1:n.1108+120_1108+121del