Canonical Allele Identifier: CA2036978931
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53430013_53430014delinsTC , CM000674.2:g.53430013_53430014delinsTC GRCh38
NC_000012.11:g.53823797_53823798delinsTC , CM000674.1:g.53823797_53823798delinsTC GRCh37
NC_000012.10:g.52110064_52110065delinsTC NCBI36
NG_015981.1:g.11159_11160delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1288+35_1288+36delinsTC MANE Select ENSP00000257863.3:n.1288+35_1288+36delinsTC
ENST00000257863.8:c.1288+35_1288+36delinsTC ENSP00000257863.3:n.1288+35_1288+36delinsTC
ENST00000379791.7:c.1140+388_1140+389delinsTC ENSP00000369117.3:n.1140+388_1140+389delinsTC
ENST00000550311.5:c.1288+35_1288+36delinsTC ENSP00000446661.1:n.1288+35_1288+36delinsTC
ENST00000550839.1:c.379+35_379+36delinsTC ENSP00000455338.1:n.379+35_379+36delinsTC
ENST00000552233.5:n.911_912delinsTC
NM_001164690.1:c.1288+35_1288+36delinsTC NP_001158162.1:n.1288+35_1288+36delinsTC
NM_001164691.1:c.1140+388_1140+389delinsTC NP_001158163.1:n.1140+388_1140+389delinsTC
NM_020547.2:c.1288+35_1288+36delinsTC NP_065434.1:n.1288+35_1288+36delinsTC
XM_011538173.1:c.1348+35_1348+36delinsTC XP_011536475.1:n.1348+35_1348+36delinsTC
XM_011538174.1:c.1345+35_1345+36delinsTC XP_011536476.1:n.1345+35_1345+36delinsTC
XM_011538175.1:c.1330+35_1330+36delinsTC XP_011536477.1:n.1330+35_1330+36delinsTC
XM_011538176.1:c.1291+35_1291+36delinsTC XP_011536478.1:n.1291+35_1291+36delinsTC
XM_011538177.1:c.1270+35_1270+36delinsTC XP_011536479.1:n.1270+35_1270+36delinsTC
XM_011538178.1:c.1129+35_1129+36delinsTC XP_011536480.1:n.1129+35_1129+36delinsTC
XM_011538179.1:c.1200+388_1200+389delinsTC XP_011536481.1:n.1200+388_1200+389delinsTC
XM_011538180.1:c.1015+35_1015+36delinsTC XP_011536482.1:n.1015+35_1015+36delinsTC
XM_011538181.1:c.1012+35_1012+36delinsTC XP_011536483.1:n.1012+35_1012+36delinsTC
XM_011538182.1:c.937+35_937+36delinsTC XP_011536484.1:n.937+35_937+36delinsTC
XM_011538183.1:c.1201-133_1201-132delinsTC XP_011536485.1:n.1201-133_1201-132delinsTC
XM_011538184.1:c.1220+368_1220+369delinsTC XP_011536486.1:n.1220+368_1220+369delinsTC
XM_011538185.1:c.856-1164_856-1163delinsTC XP_011536487.1:n.856-1164_856-1163delinsTC
XM_011538186.1:c.463+35_463+36delinsTC XP_011536488.1:n.463+35_463+36delinsTC
NM_001164690.2:c.1288+35_1288+36delinsTC NP_001158162.1:n.1288+35_1288+36delinsTC
NM_001164691.2:c.1140+388_1140+389delinsTC NP_001158163.1:n.1140+388_1140+389delinsTC
NM_020547.3:c.1288+35_1288+36delinsTC MANE Select NP_065434.1:n.1288+35_1288+36delinsTC
XM_011538183.2:c.1201-133_1201-132delinsTC XP_011536485.1:n.1201-133_1201-132delinsTC
XM_011538184.2:c.1220+368_1220+369delinsTC XP_011536486.1:n.1220+368_1220+369delinsTC
XM_011538186.3:c.463+35_463+36delinsTC XP_011536488.1:n.463+35_463+36delinsTC
XM_017019179.2:c.1348+35_1348+36delinsTC XP_016874668.1:n.1348+35_1348+36delinsTC
XM_024448938.1:c.1143+388_1143+389delinsTC XP_024304706.1:n.1143+388_1143+389delinsTC
XR_002957309.1:n.1256+35_1256+36delinsTC
XR_002957310.1:n.1109-133_1109-132delinsTC
XR_002957311.1:n.1256+35_1256+36delinsTC
XR_002957312.1:n.1108+388_1108+389delinsTC