Canonical Allele Identifier: CA2619053269
Gene: AMHR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429989_53429992dup , CM000674.2:g.53429989_53429992dup GRCh38
NC_000012.11:g.53823773_53823776dup , CM000674.1:g.53823773_53823776dup GRCh37
NC_000012.10:g.52110040_52110043dup NCBI36
NG_015981.1:g.11135_11138dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1288+11_1288+14dup MANE Select ENSP00000257863.3:n.1288+11_1288+14dup
ENST00000257863.8:c.1288+11_1288+14dup ENSP00000257863.3:n.1288+11_1288+14dup
ENST00000379791.7:c.1140+364_1140+367dup ENSP00000369117.3:n.1140+364_1140+367dup
ENST00000550311.5:c.1288+11_1288+14dup ENSP00000446661.1:n.1288+11_1288+14dup
ENST00000550839.1:c.379+11_379+14dup ENSP00000455338.1:n.379+11_379+14dup
ENST00000552233.5:n.887_890dup
NM_001164690.1:c.1288+11_1288+14dup NP_001158162.1:n.1288+11_1288+14dup
NM_001164691.1:c.1140+364_1140+367dup NP_001158163.1:n.1140+364_1140+367dup
NM_020547.2:c.1288+11_1288+14dup NP_065434.1:n.1288+11_1288+14dup
XM_011538173.1:c.1348+11_1348+14dup XP_011536475.1:n.1348+11_1348+14dup
XM_011538174.1:c.1345+11_1345+14dup XP_011536476.1:n.1345+11_1345+14dup
XM_011538175.1:c.1330+11_1330+14dup XP_011536477.1:n.1330+11_1330+14dup
XM_011538176.1:c.1291+11_1291+14dup XP_011536478.1:n.1291+11_1291+14dup
XM_011538177.1:c.1270+11_1270+14dup XP_011536479.1:n.1270+11_1270+14dup
XM_011538178.1:c.1129+11_1129+14dup XP_011536480.1:n.1129+11_1129+14dup
XM_011538179.1:c.1200+364_1200+367dup XP_011536481.1:n.1200+364_1200+367dup
XM_011538180.1:c.1015+11_1015+14dup XP_011536482.1:n.1015+11_1015+14dup
XM_011538181.1:c.1012+11_1012+14dup XP_011536483.1:n.1012+11_1012+14dup
XM_011538182.1:c.937+11_937+14dup XP_011536484.1:n.937+11_937+14dup
XM_011538183.1:c.1201-157_1201-154dup XP_011536485.1:n.1201-157_1201-154dup
XM_011538184.1:c.1220+344_1220+347dup XP_011536486.1:n.1220+344_1220+347dup
XM_011538185.1:c.856-1188_856-1185dup XP_011536487.1:n.856-1188_856-1185dup
XM_011538186.1:c.463+11_463+14dup XP_011536488.1:n.463+11_463+14dup
NM_001164690.2:c.1288+11_1288+14dup NP_001158162.1:n.1288+11_1288+14dup
NM_001164691.2:c.1140+364_1140+367dup NP_001158163.1:n.1140+364_1140+367dup
NM_020547.3:c.1288+11_1288+14dup MANE Select NP_065434.1:n.1288+11_1288+14dup
XM_011538183.2:c.1201-157_1201-154dup XP_011536485.1:n.1201-157_1201-154dup
XM_011538184.2:c.1220+344_1220+347dup XP_011536486.1:n.1220+344_1220+347dup
XM_011538186.3:c.463+11_463+14dup XP_011536488.1:n.463+11_463+14dup
XM_017019179.2:c.1348+11_1348+14dup XP_016874668.1:n.1348+11_1348+14dup
XM_024448938.1:c.1143+364_1143+367dup XP_024304706.1:n.1143+364_1143+367dup
XR_002957309.1:n.1256+11_1256+14dup
XR_002957310.1:n.1109-157_1109-154dup
XR_002957311.1:n.1256+11_1256+14dup
XR_002957312.1:n.1108+364_1108+367dup